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nsv6176497

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:167

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 76 SVs from 20 studies. See in: genome view    
Submitted genomic122,185,148-122,185,314Question Mark
Overlapping variant regions from other studies: 76 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):124,947,427-124,947,593Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6176497Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,185,148122,185,314
nsv6176497RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9124,947,427124,947,593

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17913995deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17913995Submitted genomicNC_000009.12:g.122
185148_122185314de
l
GRCh38 (hg38)NC_000009.12Chr9122,185,148122,185,314
nssv17913995RemappedPerfectNC_000009.11:g.124
947427_124947593de
l
GRCh37.p13First PassNC_000009.11Chr9124,947,427124,947,593

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)
nssv179139950.00242298
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