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nsv6970527

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,773

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 488 SVs from 59 studies. See in: genome view    
    Submitted genomic1,073,138-1,091,910Question Mark
    Overlapping variant regions from other studies: 488 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):1,123,138-1,141,910Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6970527Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr161,073,1381,091,910
    nsv6970527RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,123,1381,141,910

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18400099deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18400099Submitted genomicNC_000016.10:g.107
    3138_1091910del
    GRCh38 (hg38)NC_000016.10Chr161,073,1381,091,910
    nssv18400099RemappedPerfectNC_000016.9:g.1123
    138_1141910del
    GRCh37.p13First PassNC_000016.9Chr161,123,1381,141,910

    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)
    nssv184000994e-061273718
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