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nsv6982925

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:304

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 156 SVs from 29 studies. See in: genome view    
    Submitted genomic86,247,320-86,247,623Question Mark
    Overlapping variant regions from other studies: 156 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):86,280,926-86,281,229Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6982925Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1686,247,32086,247,623
    nsv6982925RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1686,280,92686,281,229

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18625395duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18625395Submitted genomicNC_000016.10:g.862
    47320_86247623dup
    GRCh38 (hg38)NC_000016.10Chr1686,247,32086,247,623
    nssv18625395RemappedPerfectNC_000016.9:g.8628
    0926_86281229dup
    GRCh37.p13First PassNC_000016.9Chr1686,280,92686,281,229

    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)
    nssv186253954e-061231844
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