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nsv7066677

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:100,928

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 927 SVs from 82 studies. See in: genome view    
    Submitted genomic63,739,500-63,840,427Question Mark
    Overlapping variant regions from other studies: 927 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):64,313,633-64,414,560Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066677Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1363,739,50063,840,427
    nsv7066677RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1364,313,63364,414,560

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753701inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753701Submitted genomicNC_000013.11:g.637
    39500_63840427inv
    GRCh38 (hg38)NC_000013.11Chr1363,739,50063,840,427
    nssv18753701RemappedPerfectNC_000013.10:g.643
    13633_64414560inv
    GRCh37.p13First PassNC_000013.10Chr1364,313,63364,414,560

    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)
    nssv187537010.037723260648
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