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nsv5519016

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,791

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 28 studies. See in: genome view    
Submitted genomic64,382,822-64,384,612Question Mark
Overlapping variant regions from other studies: 105 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):64,675,021-64,676,811Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5519016Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1564,382,82264,384,612
nsv5519016RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1564,675,02164,676,811

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704197deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704197Submitted genomicNC_000015.10:g.643
82822_64384612del
GRCh38 (hg38)NC_000015.10Chr1564,382,82264,384,612
nssv17704197RemappedPerfectNC_000015.9:g.6467
5021_64676811del
GRCh37.p13First PassNC_000015.9Chr1564,675,02164,676,811

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)
nssv17704197<0.00146404
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