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nsv7053920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,717,866

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7676 SVs from 101 studies. See in: genome view    
    Submitted genomic67,470,120-71,187,985Question Mark
    Overlapping variant regions from other studies: 7676 SVs from 101 studies. See in: genome view    
    Remapped(Score: Perfect):67,935,803-71,653,668Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr167,470,12071,187,985
    nsv7053920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr167,935,80371,653,668

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761729inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761729Submitted genomicNC_000001.11:g.674
    70120_71187985inv
    GRCh38 (hg38)NC_000001.11Chr167,470,12071,187,985
    nssv18761729RemappedPerfectNC_000001.10:g.679
    35803_71653668inv
    GRCh37.p13First PassNC_000001.10Chr167,935,80371,653,668

    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)
    nssv187617296.4e-0518275244
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