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nsv6940716

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61,310

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 226 SVs from 35 studies. See in: genome view    
    Submitted genomic55,568,162-55,629,471Question Mark
    Overlapping variant regions from other studies: 226 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):56,034,880-56,096,189Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6940716Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1455,568,16255,629,471
    nsv6940716RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1456,034,88056,096,189

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18613736duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18613736Submitted genomicNC_000014.9:g.5556
    8162_55629471dup
    GRCh38 (hg38)NC_000014.9Chr1455,568,16255,629,471
    nssv18613736RemappedPerfectNC_000014.8:g.5603
    4880_56096189dup
    GRCh37.p13First PassNC_000014.8Chr1456,034,88056,096,189

    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)
    nssv186137364e-061275752
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