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nsv6884052

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:247,079

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 712 SVs from 60 studies. See in: genome view    
    Submitted genomic114,876,531-115,123,609Question Mark
    Overlapping variant regions from other studies: 554 SVs from 59 studies. See in: genome view    
    Remapped(Score: Pass):116,636,290-116,786,295Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6884052Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10114,876,531115,123,609
    nsv6884052RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10116,636,290116,786,295

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18574105duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18574105Submitted genomicNC_000010.11:g.114
    876531_115123609du
    p
    GRCh38 (hg38)NC_000010.11Chr10114,876,531115,123,609
    nssv18574105RemappedPassNC_000010.10:g.116
    636290_116786295du
    p
    GRCh37.p13First PassNC_000010.10Chr10116,636,290116,786,295

    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)
    nssv185741051.8e-055271738
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