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nsv6992192

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:129,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 353 SVs from 55 studies. See in: genome view    
    Submitted genomic50,421,701-50,551,300Question Mark
    Overlapping variant regions from other studies: 353 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):50,455,612-50,585,211Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992192Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1650,421,70150,551,300
    nsv6992192RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1650,455,61250,585,211

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18624335duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18624335Submitted genomicNC_000016.10:g.504
    21701_50551300dup
    GRCh38 (hg38)NC_000016.10Chr1650,421,70150,551,300
    nssv18624335RemappedPerfectNC_000016.9:g.5045
    5612_50585211dup
    GRCh37.p13First PassNC_000016.9Chr1650,455,61250,585,211

    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)
    nssv186243354e-061273310
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