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nsv7060863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,769,338

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15810 SVs from 116 studies. See in: genome view    
    Submitted genomic127,697,992-132,467,329Question Mark
    Overlapping variant regions from other studies: 15603 SVs from 116 studies. See in: genome view    
    Remapped(Score: Good):129,496,256-134,280,833Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060863Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10127,697,992132,467,329
    nsv7060863RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10129,496,256134,280,833

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736818inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736818Submitted genomicNC_000010.11:g.127
    697992_132467329in
    v
    GRCh38 (hg38)NC_000010.11Chr10127,697,992132,467,329
    nssv18736818RemappedGoodNC_000010.10:g.129
    496256_134280833in
    v
    GRCh37.p13First PassNC_000010.10Chr10129,496,256134,280,833

    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)
    nssv187368187e-062275090
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