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nsv7051964

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,856,891

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8015 SVs from 101 studies. See in: genome view    
    Submitted genomic67,266,655-71,123,545Question Mark
    Overlapping variant regions from other studies: 8015 SVs from 101 studies. See in: genome view    
    Remapped(Score: Perfect):67,732,338-71,589,228Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051964Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr167,266,65571,123,545
    nsv7051964RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr167,732,33871,589,228

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761727inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761727Submitted genomicNC_000001.11:g.672
    66655_71123545inv
    GRCh38 (hg38)NC_000001.11Chr167,266,65571,123,545
    nssv18761727RemappedPerfectNC_000001.10:g.677
    32338_71589228inv
    GRCh37.p13First PassNC_000001.10Chr167,732,33871,589,228

    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)
    nssv187617274e-061276268
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