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nsv7066523

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,893,426

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5225 SVs from 100 studies. See in: genome view    
    Submitted genomic36,977,322-38,870,747Question Mark
    Overlapping variant regions from other studies: 5195 SVs from 106 studies. See in: genome view    
    Remapped(Score: Pass):35,372,677-37,027,000Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066523Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1736,977,32238,870,747
    nsv7066523RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1735,372,67737,027,000

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757236inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757236Submitted genomicNC_000017.11:g.369
    77322_38870747inv
    GRCh38 (hg38)NC_000017.11Chr1736,977,32238,870,747
    nssv18757236RemappedPassNC_000017.10:g.353
    72677_37027000inv
    GRCh37.p13First PassNC_000017.10Chr1735,372,67737,027,000

    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)
    nssv187572361.1e-053274828
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