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nsv5522653

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60,442

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 244 SVs from 49 studies. See in: genome view    
Submitted genomic64,757,693-64,818,134Question Mark
Overlapping variant regions from other studies: 244 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):62,753,811-62,814,252Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5522653Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1764,757,69364,818,134
nsv5522653RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1762,753,81162,814,252

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714088deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714088Submitted genomicNC_000017.11:g.647
57693_64818134del
GRCh38 (hg38)NC_000017.11Chr1764,757,69364,818,134
nssv17714088RemappedPerfectNC_000017.10:g.627
53811_62814252del
GRCh37.p13First PassNC_000017.10Chr1762,753,81162,814,252

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)
nssv17714088<0.00116404
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