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nsv5518550

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,586

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 117 SVs from 24 studies. See in: genome view    
Submitted genomic37,123,129-37,124,714Question Mark
Overlapping variant regions from other studies: 117 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):35,751,532-35,753,117Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518550Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2037,123,12937,124,714
nsv5518550RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2035,751,53235,753,117

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732248duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732248Submitted genomicNC_000020.11:g.371
23129_37124714dup
GRCh38 (hg38)NC_000020.11Chr2037,123,12937,124,714
nssv17732248RemappedPerfectNC_000020.10:g.357
51532_35753117dup
GRCh37.p13First PassNC_000020.10Chr2035,751,53235,753,117

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)
nssv17732248<0.00116404
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