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nsv7054149

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,244,433

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10761 SVs from 109 studies. See in: genome view    
    Submitted genomic79,216,923-83,461,355Question Mark
    Overlapping variant regions from other studies: 10761 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):80,138,077-84,382,508Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054149Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr479,216,92383,461,355
    nsv7054149RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr480,138,07784,382,508

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776328inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776328Submitted genomicNC_000004.12:g.792
    16923_83461355inv
    GRCh38 (hg38)NC_000004.12Chr479,216,92383,461,355
    nssv18776328RemappedPerfectNC_000004.11:g.801
    38077_84382508inv
    GRCh37.p13First PassNC_000004.11Chr480,138,07784,382,508

    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)
    nssv187763287e-062276268
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