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nsv6534918

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:158,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 897 SVs from 75 studies. See in: genome view    
    Submitted genomic36,330,301-36,488,900Question Mark
    Overlapping variant regions from other studies: 897 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):36,821,203-36,979,802Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6534918Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,330,30136,488,900
    nsv6534918RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,821,20336,979,802

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18197806duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18197806Submitted genomicNC_000019.10:g.363
    30301_36488900dup
    GRCh38 (hg38)NC_000019.10Chr1936,330,30136,488,900
    nssv18197806RemappedPerfectNC_000019.9:g.3682
    1203_36979802dup
    GRCh37.p13First PassNC_000019.9Chr1936,821,20336,979,802

    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)
    nssv18197806<0.001226284
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