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nsv6907833

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71,925

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 347 SVs from 46 studies. See in: genome view    
    Submitted genomic130,339,445-130,411,369Question Mark
    Overlapping variant regions from other studies: 347 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):130,209,340-130,281,264Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6907833Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11130,339,445130,411,369
    nsv6907833RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11130,209,340130,281,264

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18583974duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18583974Submitted genomicNC_000011.10:g.130
    339445_130411369du
    p
    GRCh38 (hg38)NC_000011.10Chr11130,339,445130,411,369
    nssv18583974RemappedPerfectNC_000011.9:g.1302
    09340_130281264dup
    GRCh37.p13First PassNC_000011.9Chr11130,209,340130,281,264

    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)
    nssv185839744e-061275990
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