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nsv6846670

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:182

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 15 studies. See in: genome view    
    Submitted genomic58,032,655-58,032,836Question Mark
    Overlapping variant regions from other studies: 103 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):58,945,214-58,945,395Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6846670Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr858,032,65558,032,836
    nsv6846670RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr858,945,21458,945,395

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739140duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739140Submitted genomicNC_000008.11:g.580
    32655_58032836dup
    GRCh38 (hg38)NC_000008.11Chr858,032,65558,032,836
    nssv18739140RemappedPerfectNC_000008.10:g.589
    45214_58945395dup
    GRCh37.p13First PassNC_000008.10Chr858,945,21458,945,395

    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)
    nssv187391405e-0512234816
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