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nsv6975912

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,143

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 20 studies. See in: genome view    
    Submitted genomic45,505,926-45,507,068Question Mark
    Overlapping variant regions from other studies: 117 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):45,798,124-45,799,266Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6975912Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1545,505,92645,507,068
    nsv6975912RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1545,798,12445,799,266

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615672duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615672Submitted genomicNC_000015.10:g.455
    05926_45507068dup
    GRCh38 (hg38)NC_000015.10Chr1545,505,92645,507,068
    nssv18615672RemappedPerfectNC_000015.9:g.4579
    8124_45799266dup
    GRCh37.p13First PassNC_000015.9Chr1545,798,12445,799,266

    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)
    nssv186156724e-061262852
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