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nsv6511818

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134,072

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 503 SVs from 55 studies. See in: genome view    
    Submitted genomic41,326,682-41,460,753Question Mark
    Overlapping variant regions from other studies: 503 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):41,618,880-41,752,951Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6511818Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1541,326,68241,460,753
    nsv6511818RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,618,88041,752,951

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18187626duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18187626Submitted genomicNC_000015.10:g.413
    26682_41460753dup
    GRCh38 (hg38)NC_000015.10Chr1541,326,68241,460,753
    nssv18187626RemappedPerfectNC_000015.9:g.4161
    8880_41752951dup
    GRCh37.p13First PassNC_000015.9Chr1541,618,88041,752,951

    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)
    nssv18187626<0.001139272
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