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nsv6894392

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 186 SVs from 42 studies. See in: genome view    
    Submitted genomic920,601-924,900Question Mark
    Overlapping variant regions from other studies: 186 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):920,601-924,900Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6894392Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11920,601924,900
    nsv6894392RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11920,601924,900

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18354674deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18354674Submitted genomicNC_000011.10:g.920
    601_924900del
    GRCh38 (hg38)NC_000011.10Chr11920,601924,900
    nssv18354674RemappedPerfectNC_000011.9:g.9206
    01_924900del
    GRCh37.p13First PassNC_000011.9Chr11920,601924,900

    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)
    nssv18354674<0.001218252580
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