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nsv6833100

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:213,426

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 458 SVs from 58 studies. See in: genome view    
    Submitted genomic86,825,568-87,038,993Question Mark
    Overlapping variant regions from other studies: 458 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):86,454,884-86,668,309Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6833100Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr786,825,56887,038,993
    nsv6833100RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr786,454,88486,668,309

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18726158duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18726158Submitted genomicNC_000007.14:g.868
    25568_87038993dup
    GRCh38 (hg38)NC_000007.14Chr786,825,56887,038,993
    nssv18726158RemappedPerfectNC_000007.13:g.864
    54884_86668309dup
    GRCh37.p13First PassNC_000007.13Chr786,454,88486,668,309

    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)
    nssv187261584e-061275388
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