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nsv5476017

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:158,845

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 649 SVs from 66 studies. See in: genome view    
Submitted genomic55,808,595-55,967,439Question Mark
Overlapping variant regions from other studies: 649 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):56,721,154-56,879,998Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5476017Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr855,808,59555,967,439
nsv5476017RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr856,721,15456,879,998

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17012396duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17012396Submitted genomicNC_000008.11:g.558
08595_55967439dup
GRCh38 (hg38)NC_000008.11Chr855,808,59555,967,439
nssv17012396RemappedPerfectNC_000008.10:g.567
21154_56879998dup
GRCh37.p13First PassNC_000008.10Chr856,721,15456,879,998

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)
nssv17012396<0.00116404
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