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nsv7062541

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,668,832

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5650 SVs from 112 studies. See in: genome view    
    Submitted genomic63,273,090-64,941,921Question Mark
    Overlapping variant regions from other studies: 5650 SVs from 112 studies. See in: genome view    
    Remapped(Score: Perfect):63,847,223-65,516,053Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062541Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1363,273,09064,941,921
    nsv7062541RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1363,847,22365,516,053

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753684inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753684Submitted genomicNC_000013.11:g.632
    73090_64941921inv
    GRCh38 (hg38)NC_000013.11Chr1363,273,09064,941,921
    nssv18753684RemappedPerfectNC_000013.10:g.638
    47223_65516053inv
    GRCh37.p13First PassNC_000013.10Chr1363,847,22365,516,053

    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)
    nssv187536842.5e-057276266
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