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nsv5476557

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,402

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 275 SVs from 33 studies. See in: genome view    
Submitted genomic124,639,120-124,681,521Question Mark
Overlapping variant regions from other studies: 275 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):125,651,361-125,693,762Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5476557Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8124,639,120124,681,521
nsv5476557RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8125,651,361125,693,762

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17017140duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17017140Submitted genomicNC_000008.11:g.124
639120_124681521du
p
GRCh38 (hg38)NC_000008.11Chr8124,639,120124,681,521
nssv17017140RemappedPerfectNC_000008.10:g.125
651361_125693762du
p
GRCh37.p13First PassNC_000008.10Chr8125,651,361125,693,762

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17017140<0.00116404
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