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nsv5424855

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,197

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 24 studies. See in: genome view    
Submitted genomic95,169,584-95,170,780Question Mark
Overlapping variant regions from other studies: 115 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):95,635,140-95,636,336Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424855Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr195,169,58495,170,780
nsv5424855RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr195,635,14095,636,336

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17683921deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17683921Submitted genomicNC_000001.11:g.951
69584_95170780del
GRCh38 (hg38)NC_000001.11Chr195,169,58495,170,780
nssv17683921RemappedPerfectNC_000001.10:g.956
35140_95636336del
GRCh37.p13First PassNC_000001.10Chr195,635,14095,636,336

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)
nssv17683921<0.00116404
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