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nsv6997035

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,566,501

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4249 SVs from 104 studies. See in: genome view    
    Submitted genomic9,981,556-11,548,056Question Mark
    Overlapping variant regions from other studies: 4249 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):9,884,873-11,451,373Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6997035Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr179,981,55611,548,056
    nsv6997035RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr179,884,87311,451,373

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18632290duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18632290Submitted genomicNC_000017.11:g.998
    1556_11548056dup
    GRCh38 (hg38)NC_000017.11Chr179,981,55611,548,056
    nssv18632290RemappedPerfectNC_000017.10:g.988
    4873_11451373dup
    GRCh37.p13First PassNC_000017.10Chr179,884,87311,451,373

    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)
    nssv186322904e-061275890
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