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nsv6961537

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,562

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
    Submitted genomic9,451,264-9,470,825Question Mark
    Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):9,545,121-9,564,682Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6961537Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr169,451,2649,470,825
    nsv6961537RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr169,545,1219,564,682

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18405851deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18405851Submitted genomicNC_000016.10:g.945
    1264_9470825del
    GRCh38 (hg38)NC_000016.10Chr169,451,2649,470,825
    nssv18405851RemappedPerfectNC_000016.9:g.9545
    121_9564682del
    GRCh37.p13First PassNC_000016.9Chr169,545,1219,564,682

    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)
    nssv184058512.5e-057276016
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