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nsv7068192

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,873,621

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17791 SVs from 124 studies. See in: genome view    
    Submitted genomic118,910,158-125,783,778Question Mark
    Overlapping variant regions from other studies: 17678 SVs from 124 studies. See in: genome view    
    Remapped(Score: Good):120,669,670-127,472,347Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068192Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10118,910,158125,783,778
    nsv7068192RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10120,669,670127,472,347

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18747236inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18747236Submitted genomicNC_000010.11:g.118
    910158_125783778in
    v
    GRCh38 (hg38)NC_000010.11Chr10118,910,158125,783,778
    nssv18747236RemappedGoodNC_000010.10:g.120
    669670_127472347in
    v
    GRCh37.p13First PassNC_000010.10Chr10120,669,670127,472,347

    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)
    nssv18747236<0.00130274670
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