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nsv6914621

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,541

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 28 studies. See in: genome view    
    Submitted genomic22,701,280-22,703,820Question Mark
    Overlapping variant regions from other studies: 92 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):22,722,826-22,725,366Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6914621Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1122,701,28022,703,820
    nsv6914621RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1122,722,82622,725,366

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18345534deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18345534Submitted genomicNC_000011.10:g.227
    01280_22703820del
    GRCh38 (hg38)NC_000011.10Chr1122,701,28022,703,820
    nssv18345534RemappedPerfectNC_000011.9:g.2272
    2826_22725366del
    GRCh37.p13First PassNC_000011.9Chr1122,722,82622,725,366

    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)
    nssv183455346.4e-0518276066
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