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nsv6916075

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:489,955

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1829 SVs from 96 studies. See in: genome view    
    Submitted genomic107,601,350-108,091,304Question Mark
    Overlapping variant regions from other studies: 1830 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):107,472,076-107,962,031Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6916075Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11107,601,350108,091,304
    nsv6916075RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11107,472,076107,962,031

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18583564duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18583564Submitted genomicNC_000011.10:g.107
    601350_108091304du
    p
    GRCh38 (hg38)NC_000011.10Chr11107,601,350108,091,304
    nssv18583564RemappedPerfectNC_000011.9:g.1074
    72076_107962031dup
    GRCh37.p13First PassNC_000011.9Chr11107,472,076107,962,031

    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)
    nssv185835644e-061275768
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