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nsv6966682

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:626

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 244 SVs from 33 studies. See in: genome view    
    Submitted genomic1,856,286-1,856,911Question Mark
    Overlapping variant regions from other studies: 244 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):1,906,287-1,906,912Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6966682Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr161,856,2861,856,911
    nsv6966682RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,906,2871,906,912

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400320deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400320Submitted genomicNC_000016.10:g.185
    6286_1856911del
    GRCh38 (hg38)NC_000016.10Chr161,856,2861,856,911
    nssv18400320RemappedPerfectNC_000016.9:g.1906
    287_1906912del
    GRCh37.p13First PassNC_000016.9Chr161,906,2871,906,912

    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)
    nssv18400320<0.00189235012
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