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nsv6900084

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,744

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 60 SVs from 23 studies. See in: genome view    
    Submitted genomic10,311,136-10,315,879Question Mark
    Overlapping variant regions from other studies: 60 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):10,332,683-10,337,426Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6900084Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1110,311,13610,315,879
    nsv6900084RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1110,332,68310,337,426

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18578842duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18578842Submitted genomicNC_000011.10:g.103
    11136_10315879dup
    GRCh38 (hg38)NC_000011.10Chr1110,311,13610,315,879
    nssv18578842RemappedPerfectNC_000011.9:g.1033
    2683_10337426dup
    GRCh37.p13First PassNC_000011.9Chr1110,332,68310,337,426

    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)
    nssv185788427e-062275536
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