U.S. flag

An official website of the United States government

nsv469527

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98,770

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 774 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):101,783,816-101,882,585Question Mark
Overlapping variant regions from other studies: 774 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):102,324,019-102,422,788Question Mark
Overlapping variant regions from other studies: 2 SVs from 1 studies. See in: genome view    
Submitted genomic100,059,283-100,158,052Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469527RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr15101,783,816101,882,585
nsv469527RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr15102,324,019102,422,788
nsv469527Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000015.7Chr15100,059,283100,158,052

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1673275copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1673275RemappedPerfectNC_000015.10:g.(?_
101783816)_(101882
585_?)del
GRCh38.p12First PassNC_000015.10Chr15101,783,816101,882,585
nssv1673275RemappedPerfectNC_000015.9:g.(?_1
02324019)_(1024227
88_?)del
GRCh37.p13First PassNC_000015.9Chr15102,324,019102,422,788
nssv1673275Submitted genomicNC_000015.7:g.(?_1
00059283)_(1001580
52_?)del
NCBI34 (hg16)NC_000015.7Chr15100,059,283100,158,052

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