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nsv7007952

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:203,753

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 892 SVs from 73 studies. See in: genome view    
    Submitted genomic19,916,804-20,120,556Question Mark
    Overlapping variant regions from other studies: 741 SVs from 70 studies. See in: genome view    
    Remapped(Score: Pass):20,027,613-20,193,556Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7007952Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1919,916,80420,120,556
    nsv7007952RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1920,027,61320,193,556

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18637220duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18637220Submitted genomicNC_000019.10:g.199
    16804_20120556dup
    GRCh38 (hg38)NC_000019.10Chr1919,916,80420,120,556
    nssv18637220RemappedPassNC_000019.9:g.2002
    7613_20193556dup
    GRCh37.p13First PassNC_000019.9Chr1920,027,61320,193,556

    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)
    nssv186372204e-061275546
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