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nsv7058808

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,377,581

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15343 SVs from 126 studies. See in: genome view    
    Submitted genomic57,953,150-64,330,730Question Mark
    Overlapping variant regions from other studies: 15343 SVs from 126 studies. See in: genome view    
    Remapped(Score: Perfect):58,346,933-64,724,510Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058808Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1257,953,15064,330,730
    nsv7058808RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1258,346,93364,724,510

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752408inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752408Submitted genomicNC_000012.12:g.579
    53150_64330730inv
    GRCh38 (hg38)NC_000012.12Chr1257,953,15064,330,730
    nssv18752408RemappedPerfectNC_000012.11:g.583
    46933_64724510inv
    GRCh37.p13First PassNC_000012.11Chr1258,346,93364,724,510

    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)
    nssv187524081.1e-053274990
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