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nsv7042745

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:88,555

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 401 SVs from 40 studies. See in: genome view    
    Submitted genomic13,249,961-13,338,515Question Mark
    Overlapping variant regions from other studies: 401 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):13,250,193-13,338,747Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042745Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr613,249,96113,338,515
    nsv7042745RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr613,250,19313,338,747

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776634inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776634Submitted genomicNC_000006.12:g.132
    49961_13338515inv
    GRCh38 (hg38)NC_000006.12Chr613,249,96113,338,515
    nssv18776634RemappedPerfectNC_000006.11:g.132
    50193_13338747inv
    GRCh37.p13First PassNC_000006.11Chr613,250,19313,338,747

    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)
    nssv187766344e-061276268
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