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nsv6812189

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69,896

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 489 SVs from 66 studies. See in: genome view    
    Submitted genomic17,458,678-17,528,573Question Mark
    Overlapping variant regions from other studies: 489 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):17,498,302-17,568,197Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6812189Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr717,458,67817,528,573
    nsv6812189RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr717,498,30217,568,197

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18724191duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18724191Submitted genomicNC_000007.14:g.174
    58678_17528573dup
    GRCh38 (hg38)NC_000007.14Chr717,458,67817,528,573
    nssv18724191RemappedPerfectNC_000007.13:g.174
    98302_17568197dup
    GRCh37.p13First PassNC_000007.13Chr717,498,30217,568,197

    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)
    nssv187241914e-061275628
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