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nsv5523632

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23,875

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 265 SVs from 55 studies. See in: genome view    
Submitted genomic84,196,000-84,219,874Question Mark
Overlapping variant regions from other studies: 265 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):84,864,752-84,888,626Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523632Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1584,196,00084,219,874
nsv5523632RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1584,864,75284,888,626

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702628deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702628Submitted genomicNC_000015.10:g.841
96000_84219874del
GRCh38 (hg38)NC_000015.10Chr1584,196,00084,219,874
nssv17702628RemappedPerfectNC_000015.9:g.8486
4752_84888626del
GRCh37.p13First PassNC_000015.9Chr1584,864,75284,888,626

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)
nssv177026280.011635710
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