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nsv6431654

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,533

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 264 SVs from 41 studies. See in: genome view    
    Submitted genomic21,240,366-21,254,898Question Mark
    Overlapping variant regions from other studies: 270 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):21,240,365-21,254,897Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6431654Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr921,240,36621,254,898
    nsv6431654RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr921,240,36521,254,897

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18175753deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18175753Submitted genomicNC_000009.12:g.212
    40366_21254898del
    GRCh38 (hg38)NC_000009.12Chr921,240,36621,254,898
    nssv18175753RemappedPerfectNC_000009.11:g.212
    40365_21254897del
    GRCh37.p13First PassNC_000009.11Chr921,240,36521,254,897

    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)
    nssv18175753<0.001139254
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