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nsv3112524

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,513,785

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 4251 SVs from 96 studies. See in: genome view    
Remapped(Score: Perfect):69,499,909-71,013,693Question Mark
Overlapping variant regions from other studies: 936 SVs from 59 studies. See in: genome view    
Remapped(Score: Pass):1-794,347Question Mark
Overlapping variant regions from other studies: 398 SVs from 46 studies. See in: genome view    
Remapped(Score: Pass):397,152-1,248,408Question Mark
Overlapping variant regions from other studies: 4253 SVs from 96 studies. See in: genome view    
Submitted genomic68,795,736-70,309,520Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv3112524RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr569,499,90971,013,693
nsv3112524RemappedPassGRCh38.p12ALT_REF_LOCI_2Second PassNT_187651.1Chr5|NT_18
7651.1
1794,347
nsv3112524RemappedPassGRCh38.p12ALT_REF_LOCI_1Second PassNW_003315917.2Chr5|NW_00
3315917.2
397,1521,248,408
nsv3112524Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr568,795,73670,309,520

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14109440duplicationsample346Oligo aCGHProbe signal intensity74

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv14109440RemappedPassNT_187651.1:g.(?_1
)_(794347_?)dup
GRCh38.p12Second PassNT_187651.1Chr5|NT_18
7651.1
1794,347
nssv14109440RemappedPassNW_003315917.2:g.(
?_397152)_(1248408
_?)dup
GRCh38.p12Second PassNW_003315917.2Chr5|NW_00
3315917.2
397,1521,248,408
nssv14109440RemappedPerfectNC_000005.10:g.(?_
69499909)_(7101369
3_?)dup
GRCh38.p12First PassNC_000005.10Chr569,499,90971,013,693
nssv14109440Submitted genomicNC_000005.9:g.(?_6
8795736)_(70309520
_?)dup
GRCh37 (hg19)NC_000005.9Chr568,795,73670,309,520

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

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