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nsv7044198

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,934,055

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 14011 SVs from 123 studies. See in: genome view    
    Submitted genomic93,856,097-99,790,151Question Mark
    Overlapping variant regions from other studies: 14012 SVs from 123 studies. See in: genome view    
    Remapped(Score: Perfect):93,191,803-99,125,855Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044198Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr593,856,09799,790,151
    nsv7044198RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr593,191,80399,125,855

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777007inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777007Submitted genomicNC_000005.10:g.938
    56097_99790151inv
    GRCh38 (hg38)NC_000005.10Chr593,856,09799,790,151
    nssv18777007RemappedPerfectNC_000005.9:g.9319
    1803_99125855inv
    GRCh37.p13First PassNC_000005.9Chr593,191,80399,125,855

    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)
    nssv187770074e-061276266
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