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nsv5529934

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,753

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 275 SVs from 47 studies. See in: genome view    
Submitted genomic63,876,118-63,883,870Question Mark
Overlapping variant regions from other studies: 275 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):61,953,478-61,961,230Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529934Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1763,876,11863,883,870
nsv5529934RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1761,953,47861,961,230

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714034deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714034Submitted genomicNC_000017.11:g.638
76118_63883870del
GRCh38 (hg38)NC_000017.11Chr1763,876,11863,883,870
nssv17714034RemappedPerfectNC_000017.10:g.619
53478_61961230del
GRCh37.p13First PassNC_000017.10Chr1761,953,47861,961,230

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)
nssv177140340.003196402
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