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nsv2794634

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,342

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 759 SVs from 81 studies. See in: genome view    
Submitted genomic76,592,257-76,604,598Question Mark
Overlapping variant regions from other studies: 759 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):76,884,598-76,896,939Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2794634Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1576,592,25776,604,598
nsv2794634RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1576,884,59876,896,939

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13700021deletionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13700021Submitted genomicNC_000015.10:g.765
92257_76604598del1
2342
GRCh38 (hg38)NC_000015.10Chr1576,592,25776,604,598
nssv13700021RemappedPerfectNC_000015.9:g.7688
4598_76896939del12
342
GRCh37.p13First PassNC_000015.9Chr1576,884,59876,896,939

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)
nssv137000210.4062664
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