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nsv6899903

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,380

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 169 SVs from 51 studies. See in: genome view    
    Submitted genomic5,838,281-5,849,660Question Mark
    Overlapping variant regions from other studies: 169 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):5,859,511-5,870,890Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6899903Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr115,838,2815,849,660
    nsv6899903RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr115,859,5115,870,890

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18352714deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18352714Submitted genomicNC_000011.10:g.583
    8281_5849660del
    GRCh38 (hg38)NC_000011.10Chr115,838,2815,849,660
    nssv18352714RemappedPerfectNC_000011.9:g.5859
    511_5870890del
    GRCh37.p13First PassNC_000011.9Chr115,859,5115,870,890

    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)
    nssv183527141.4e-054275894
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