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nsv7073041

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:253,488

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 798 SVs from 61 studies. See in: genome view    
    Submitted genomic67,001,693-67,255,180Question Mark
    Overlapping variant regions from other studies: 798 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):67,913,928-68,167,415Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073041Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr867,001,69367,255,180
    nsv7073041RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr867,913,92868,167,415

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784961inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784961Submitted genomicNC_000008.11:g.670
    01693_67255180inv
    GRCh38 (hg38)NC_000008.11Chr867,001,69367,255,180
    nssv18784961RemappedPerfectNC_000008.10:g.679
    13928_68167415inv
    GRCh37.p13First PassNC_000008.10Chr867,913,92868,167,415

    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)
    nssv187849614e-061276268
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