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nsv5514759

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,967

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 160 SVs from 27 studies. See in: genome view    
Submitted genomic62,637,101-62,655,067Question Mark
Overlapping variant regions from other studies: 160 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):60,714,462-60,732,428Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514759Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1762,637,10162,655,067
nsv5514759RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1760,714,46260,732,428

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713945duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713945Submitted genomicNC_000017.11:g.626
37101_62655067dup
GRCh38 (hg38)NC_000017.11Chr1762,637,10162,655,067
nssv17713945RemappedPerfectNC_000017.10:g.607
14462_60732428dup
GRCh37.p13First PassNC_000017.10Chr1760,714,46260,732,428

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)
nssv17713945<0.00116404
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