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nsv6449853

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:411

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 157 SVs from 41 studies. See in: genome view    
    Submitted genomic1,686,682-1,687,092Question Mark
    Overlapping variant regions from other studies: 157 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):1,707,912-1,708,322Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6449853Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr111,686,6821,687,092
    nsv6449853RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr111,707,9121,708,322

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18178266duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18178266Submitted genomicNC_000011.10:g.168
    6682_1687092dup
    GRCh38 (hg38)NC_000011.10Chr111,686,6821,687,092
    nssv18178266RemappedPerfectNC_000011.9:g.1707
    912_1708322dup
    GRCh37.p13First PassNC_000011.9Chr111,707,9121,708,322

    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)
    nssv181782660.0012723748
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