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nsv6905962

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:503

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 192 SVs from 23 studies. See in: genome view    
    Submitted genomic130,365,290-130,365,792Question Mark
    Overlapping variant regions from other studies: 192 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):130,235,185-130,235,687Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6905962Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11130,365,290130,365,792
    nsv6905962RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11130,235,185130,235,687

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586378duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586378Submitted genomicNC_000011.10:g.130
    365290_130365792du
    p
    GRCh38 (hg38)NC_000011.10Chr11130,365,290130,365,792
    nssv18586378RemappedPerfectNC_000011.9:g.1302
    35185_130235687dup
    GRCh37.p13First PassNC_000011.9Chr11130,235,185130,235,687

    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)
    nssv18586378<0.00152241408
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