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nsv7039561

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:154,805

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 491 SVs from 54 studies. See in: genome view    
    Submitted genomic112,945,161-113,099,965Question Mark
    Overlapping variant regions from other studies: 491 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):113,702,738-113,857,542Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039561Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2112,945,161113,099,965
    nsv7039561RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2113,702,738113,857,542

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767536inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767536Submitted genomicNC_000002.12:g.112
    945161_113099965in
    v
    GRCh38 (hg38)NC_000002.12Chr2112,945,161113,099,965
    nssv18767536RemappedPerfectNC_000002.11:g.113
    702738_113857542in
    v
    GRCh37.p13First PassNC_000002.11Chr2113,702,738113,857,542

    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)
    nssv187675365.4e-0515274112
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