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nsv5526337

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:185

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 191 SVs from 30 studies. See in: genome view    
Submitted genomic54,305,498-54,305,682Question Mark
Overlapping variant regions from other studies: 191 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):51,831,868-51,832,052Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526337Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1854,305,49854,305,682
nsv5526337RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1851,831,86851,832,052

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17718321deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17718321Submitted genomicNC_000018.10:g.543
05498_54305682del
GRCh38 (hg38)NC_000018.10Chr1854,305,49854,305,682
nssv17718321RemappedPerfectNC_000018.9:g.5183
1868_51832052del
GRCh37.p13First PassNC_000018.9Chr1851,831,86851,832,052

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)
nssv177183210.1368696404
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