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nsv7036065

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,189

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Submitted genomic36,567,961-36,571,149Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):35,196,364-35,199,552Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7036065Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2036,567,96136,571,149
    nsv7036065RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2035,196,36435,199,552

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18641370duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18641370Submitted genomicNC_000020.11:g.365
    67961_36571149dup
    GRCh38 (hg38)NC_000020.11Chr2036,567,96136,571,149
    nssv18641370RemappedPerfectNC_000020.10:g.351
    96364_35199552dup
    GRCh37.p13First PassNC_000020.10Chr2035,196,36435,199,552

    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)
    nssv186413704e-061274032
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