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nsv6366552

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:174,029

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 724 SVs from 60 studies. See in: genome view    
    Submitted genomic9,857,297-10,031,325Question Mark
    Overlapping variant regions from other studies: 724 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):9,898,981-10,073,009Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6366552Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr39,857,29710,031,325
    nsv6366552RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr39,898,98110,073,009

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18211292duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18211292Submitted genomicNC_000003.12:g.985
    7297_10031325dup
    GRCh38 (hg38)NC_000003.12Chr39,857,29710,031,325
    nssv18211292RemappedPerfectNC_000003.11:g.989
    8981_10073009dup
    GRCh37.p13First PassNC_000003.11Chr39,898,98110,073,009

    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)
    nssv18211292<0.001139282
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