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nsv5505173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,721

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 26 studies. See in: genome view    
Submitted genomic76,768,749-76,772,469Question Mark
Overlapping variant regions from other studies: 108 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):77,235,092-77,238,812Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5505173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1476,768,74976,772,469
nsv5505173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1477,235,09277,238,812

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17697978deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17697978Submitted genomicNC_000014.9:g.7676
8749_76772469del
GRCh38 (hg38)NC_000014.9Chr1476,768,74976,772,469
nssv17697978RemappedPerfectNC_000014.8:g.7723
5092_77238812del
GRCh37.p13First PassNC_000014.8Chr1477,235,09277,238,812

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)
nssv17697978<0.00116404
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