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nsv6808052

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:778

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 18 studies. See in: genome view    
    Submitted genomic109,389,671-109,390,448Question Mark
    Overlapping variant regions from other studies: 101 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):109,710,874-109,711,651Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6808052Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6109,389,671109,390,448
    nsv6808052RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6109,710,874109,711,651

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18708975duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18708975Submitted genomicNC_000006.12:g.109
    389671_109390448du
    p
    GRCh38 (hg38)NC_000006.12Chr6109,389,671109,390,448
    nssv18708975RemappedPerfectNC_000006.11:g.109
    710874_109711651du
    p
    GRCh37.p13First PassNC_000006.11Chr6109,710,874109,711,651

    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)
    nssv187089754e-061247850
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