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nsv7076942

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,153

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 32 studies. See in: genome view    
    Submitted genomic67,993,265-68,009,417Question Mark
    Overlapping variant regions from other studies: 155 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):68,027,168-68,043,320Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076942Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1667,993,26568,009,417
    nsv7076942RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1668,027,16868,043,320

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758174inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758174Submitted genomicNC_000016.10:g.679
    93265_68009417inv
    GRCh38 (hg38)NC_000016.10Chr1667,993,26568,009,417
    nssv18758174RemappedPerfectNC_000016.9:g.6802
    7168_68043320inv
    GRCh37.p13First PassNC_000016.9Chr1668,027,16868,043,320

    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)
    nssv187581741.4e-054274338
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