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nsv6972122

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:176,965

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1463 SVs from 86 studies. See in: genome view    
    Submitted genomic971,585-1,148,549Question Mark
    Overlapping variant regions from other studies: 1463 SVs from 86 studies. See in: genome view    
    Remapped(Score: Perfect):1,021,585-1,198,549Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6972122Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr16971,5851,148,549
    nsv6972122RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,021,5851,198,549

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18625454duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18625454Submitted genomicNC_000016.10:g.971
    585_1148549dup
    GRCh38 (hg38)NC_000016.10Chr16971,5851,148,549
    nssv18625454RemappedPerfectNC_000016.9:g.1021
    585_1198549dup
    GRCh37.p13First PassNC_000016.9Chr161,021,5851,198,549

    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)
    nssv186254544e-061275648
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