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nsv6914680

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,542

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 166 SVs from 48 studies. See in: genome view    
    Submitted genomic4,816,123-4,833,664Question Mark
    Overlapping variant regions from other studies: 166 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):4,837,353-4,854,894Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6914680Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,816,1234,833,664
    nsv6914680RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr114,837,3534,854,894

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18350243deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18350243Submitted genomicNC_000011.10:g.481
    6123_4833664del
    GRCh38 (hg38)NC_000011.10Chr114,816,1234,833,664
    nssv18350243RemappedPerfectNC_000011.9:g.4837
    353_4854894del
    GRCh37.p13First PassNC_000011.9Chr114,837,3534,854,894

    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)
    nssv183502434e-061275540
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