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nsv6842122

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,662

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 29 studies. See in: genome view    
    Submitted genomic66,459,630-66,465,291Question Mark
    Overlapping variant regions from other studies: 137 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):67,371,865-67,377,526Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6842122Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr866,459,63066,465,291
    nsv6842122RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr867,371,86567,377,526

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18555832deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18555832Submitted genomicNC_000008.11:g.664
    59630_66465291del
    GRCh38 (hg38)NC_000008.11Chr866,459,63066,465,291
    nssv18555832RemappedPerfectNC_000008.10:g.673
    71865_67377526del
    GRCh37.p13First PassNC_000008.10Chr867,371,86567,377,526

    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)
    nssv18555832<0.00135275986
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