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nsv6910090

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:132

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 15 studies. See in: genome view    
    Submitted genomic122,955,185-122,955,316Question Mark
    Overlapping variant regions from other studies: 125 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):122,825,893-122,826,024Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6910090Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11122,955,185122,955,316
    nsv6910090RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11122,825,893122,826,024

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18574805duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18574805Submitted genomicNC_000011.10:g.122
    955185_122955316du
    p
    GRCh38 (hg38)NC_000011.10Chr11122,955,185122,955,316
    nssv18574805RemappedPerfectNC_000011.9:g.1228
    25893_122826024dup
    GRCh37.p13First PassNC_000011.9Chr11122,825,893122,826,024

    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)
    nssv18574805<0.00163225976
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