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nsv6903998

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:364

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 16 studies. See in: genome view    
    Submitted genomic122,886,617-122,886,980Question Mark
    Overlapping variant regions from other studies: 131 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):122,757,325-122,757,688Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6903998Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11122,886,617122,886,980
    nsv6903998RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11122,757,325122,757,688

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18573236duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18573236Submitted genomicNC_000011.10:g.122
    886617_122886980du
    p
    GRCh38 (hg38)NC_000011.10Chr11122,886,617122,886,980
    nssv18573236RemappedPerfectNC_000011.9:g.1227
    57325_122757688dup
    GRCh37.p13First PassNC_000011.9Chr11122,757,325122,757,688

    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)
    nssv185732364e-061235882
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