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nsv7052894

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,476,265

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 16412 SVs from 119 studies. See in: genome view    
    Submitted genomic67,168,050-72,644,314Question Mark
    Overlapping variant regions from other studies: 15857 SVs from 117 studies. See in: genome view    
    Remapped(Score: Good):66,633,037-71,935,721Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052894Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr767,168,05072,644,314
    nsv7052894RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr766,633,03771,935,721

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781443inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781443Submitted genomicNC_000007.14:g.671
    68050_72644314inv
    GRCh38 (hg38)NC_000007.14Chr767,168,05072,644,314
    nssv18781443RemappedGoodNC_000007.13:g.666
    33037_71935721inv
    GRCh37.p13First PassNC_000007.13Chr766,633,03771,935,721

    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)
    nssv187814430.19447192244112
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