U.S. flag

An official website of the United States government

nsv428449

  • Variant Calls:17
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98,569

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 381 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):116,601,155-116,699,723Question Mark
Overlapping variant regions from other studies: 381 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):117,522,311-117,620,879Question Mark
Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view    
Submitted genomic117,741,759-117,840,327Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv428449RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4116,601,155116,699,723
nsv428449RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4117,522,311117,620,879
nsv428449Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr4117,741,759117,840,327

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv454581copy number gainHGDP00449BAC aCGHProbe signal intensity126
nssv454582copy number gainHGDP00450BAC aCGHProbe signal intensity88
nssv454583copy number gainHGDP00467BAC aCGHProbe signal intensity75
nssv454584copy number gainHGDP00471BAC aCGHProbe signal intensity73
nssv454585copy number gainHGDP00474BAC aCGHProbe signal intensity56
nssv454586copy number gainHGDP00984BAC aCGHProbe signal intensity75
nssv454588copy number gainHGDP00986BAC aCGHProbe signal intensity82
nssv454589copy number gainHGDP01086BAC aCGHProbe signal intensity52
nssv454590copy number gainHGDP01088BAC aCGHProbe signal intensity78
nssv454591copy number gainHGDP01093BAC aCGHProbe signal intensity95
nssv454592copy number lossNA18498BAC aCGHProbe signal intensity97
nssv454593copy number lossNA19108BAC aCGHProbe signal intensity84
nssv454594copy number gainNA19113BAC aCGHProbe signal intensity122
nssv454595copy number gainNA19147BAC aCGHProbe signal intensity75
nssv454596copy number gainNA19181BAC aCGHProbe signal intensity87
nssv454597copy number gainNA19189BAC aCGHProbe signal intensity94
nssv454599copy number gainNA19225BAC aCGHProbe signal intensity71

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv454581RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454582RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454583RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454584RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454585RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454586RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454588RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454589RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454590RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454591RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454592RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)del
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454593RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)del
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454594RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454595RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454596RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454597RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454599RemappedPerfectNC_000004.12:g.(?_
116601155)_(116699
723_?)dup
GRCh38.p12First PassNC_000004.12Chr4116,601,155116,699,723
nssv454581RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454582RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454583RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454584RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454585RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454586RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454588RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454589RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454590RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454591RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454592RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)del
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454593RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)del
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454594RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454595RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454596RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454597RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454599RemappedPerfectNC_000004.11:g.(?_
117522311)_(117620
879_?)dup
GRCh37.p13First PassNC_000004.11Chr4117,522,311117,620,879
nssv454581Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454582Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454583Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454584Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454585Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454586Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454588Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454589Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454590Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454591Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454592Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)del
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454593Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)del
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454594Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454595Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454596Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454597Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327
nssv454599Submitted genomicNC_000004.10:g.(?_
117741759)_(117840
327_?)dup
NCBI36 (hg18)NC_000004.10Chr4117,741,759117,840,327

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

Support Center