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nsv6693587

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:399,420

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 970 SVs from 70 studies. See in: genome view    
    Submitted genomic74,598,755-74,998,174Question Mark
    Overlapping variant regions from other studies: 970 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):74,825,882-75,225,301Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6693587Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr274,598,75574,998,174
    nsv6693587RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr274,825,88275,225,301

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18666869duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18666869Submitted genomicNC_000002.12:g.745
    98755_74998174dup
    GRCh38 (hg38)NC_000002.12Chr274,598,75574,998,174
    nssv18666869RemappedPerfectNC_000002.11:g.748
    25882_75225301dup
    GRCh37.p13First PassNC_000002.11Chr274,825,88275,225,301

    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)
    nssv186668697e-062275158
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