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nsv7017977

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 329 SVs from 21 studies. See in: genome view    
    Submitted genomic72,863,489-72,863,544Question Mark
    Overlapping variant regions from other studies: 329 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):70,530,724-70,530,779Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017977Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1872,863,48972,863,544
    nsv7017977RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1870,530,72470,530,779

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18637608duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18637608Submitted genomicNC_000018.10:g.728
    63489_72863544dup
    GRCh38 (hg38)NC_000018.10Chr1872,863,48972,863,544
    nssv18637608RemappedPerfectNC_000018.9:g.7053
    0724_70530779dup
    GRCh37.p13First PassNC_000018.9Chr1870,530,72470,530,779

    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)
    nssv186376081.4e-053217488
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