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nsv5529627

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,468

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 133 SVs from 28 studies. See in: genome view    
Submitted genomic4,735,868-4,738,335Question Mark
Overlapping variant regions from other studies: 133 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):4,785,869-4,788,336Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529627Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr164,735,8684,738,335
nsv5529627RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr164,785,8694,788,336

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704829deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704829Submitted genomicNC_000016.10:g.473
5868_4738335del
GRCh38 (hg38)NC_000016.10Chr164,735,8684,738,335
nssv17704829RemappedPerfectNC_000016.9:g.4785
869_4788336del
GRCh37.p13First PassNC_000016.9Chr164,785,8694,788,336

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)
nssv17704829<0.00126404
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