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nsv6888109

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:143,034

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1232 SVs from 82 studies. See in: genome view    
    Submitted genomic1,558,735-1,701,768Question Mark
    Overlapping variant regions from other studies: 1232 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):1,579,965-1,722,998Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6888109Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr111,558,7351,701,768
    nsv6888109RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr111,579,9651,722,998

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18571519duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18571519Submitted genomicNC_000011.10:g.155
    8735_1701768dup
    GRCh38 (hg38)NC_000011.10Chr111,558,7351,701,768
    nssv18571519RemappedPerfectNC_000011.9:g.1579
    965_1722998dup
    GRCh37.p13First PassNC_000011.9Chr111,579,9651,722,998

    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)
    nssv185715197e-062275672
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