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nsv7067898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:458,221

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1510 SVs from 86 studies. See in: genome view    
    Submitted genomic52,258,187-52,716,407Question Mark
    Overlapping variant regions from other studies: 1510 SVs from 86 studies. See in: genome view    
    Remapped(Score: Perfect):52,832,322-53,290,542Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1352,258,18752,716,407
    nsv7067898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1352,832,32253,290,542

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753005inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753005Submitted genomicNC_000013.11:g.522
    58187_52716407inv
    GRCh38 (hg38)NC_000013.11Chr1352,258,18752,716,407
    nssv18753005RemappedPerfectNC_000013.10:g.528
    32322_53290542inv
    GRCh37.p13First PassNC_000013.10Chr1352,832,32253,290,542

    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)
    nssv187530052.5e-057274520
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