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nsv6931262

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:161,631

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2099 SVs from 104 studies. See in: genome view    
    Submitted genomic7,782,698-7,944,328Question Mark
    Overlapping variant regions from other studies: 2099 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):7,935,294-8,096,924Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6931262Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr127,782,6987,944,328
    nsv6931262RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr127,935,2948,096,924

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18598622duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18598622Submitted genomicNC_000012.12:g.778
    2698_7944328dup
    GRCh38 (hg38)NC_000012.12Chr127,782,6987,944,328
    nssv18598622RemappedPerfectNC_000012.11:g.793
    5294_8096924dup
    GRCh37.p13First PassNC_000012.11Chr127,935,2948,096,924

    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)
    nssv185986224e-061272998
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