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nsv6777097

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:212,413

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 566 SVs from 50 studies. See in: genome view    
    Submitted genomic31,001,934-31,214,346Question Mark
    Overlapping variant regions from other studies: 566 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):31,002,041-31,214,453Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6777097Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr531,001,93431,214,346
    nsv6777097RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr531,002,04131,214,453

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18703204duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18703204Submitted genomicNC_000005.10:g.310
    01934_31214346dup
    GRCh38 (hg38)NC_000005.10Chr531,001,93431,214,346
    nssv18703204RemappedPerfectNC_000005.9:g.3100
    2041_31214453dup
    GRCh37.p13First PassNC_000005.9Chr531,002,04131,214,453

    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)
    nssv187032044e-061276252
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