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nsv5528444

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,051

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 116 SVs from 28 studies. See in: genome view    
Submitted genomic65,345,237-65,346,287Question Mark
Overlapping variant regions from other studies: 116 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):65,637,575-65,638,625Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528444Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1565,345,23765,346,287
nsv5528444RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1565,637,57565,638,625

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704272deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704272Submitted genomicNC_000015.10:g.653
45237_65346287del
GRCh38 (hg38)NC_000015.10Chr1565,345,23765,346,287
nssv17704272RemappedPerfectNC_000015.9:g.6563
7575_65638625del
GRCh37.p13First PassNC_000015.9Chr1565,637,57565,638,625

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)
nssv17704272<0.00156404
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