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nsv5523050

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 13 studies. See in: genome view    
Submitted genomic34,087,913-34,087,997Question Mark
Overlapping variant regions from other studies: 111 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):32,675,719-32,675,803Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523050Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2034,087,91334,087,997
nsv5523050RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2032,675,71932,675,803

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732064duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732064Submitted genomicNC_000020.11:g.340
87913_34087997dup
GRCh38 (hg38)NC_000020.11Chr2034,087,91334,087,997
nssv17732064RemappedPerfectNC_000020.10:g.326
75719_32675803dup
GRCh37.p13First PassNC_000020.10Chr2032,675,71932,675,803

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)
nssv17732064<0.00116404
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