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nsv6327085

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:113,833

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 399 SVs from 66 studies. See in: genome view    
    Submitted genomic70,222,207-70,336,039Question Mark
    Overlapping variant regions from other studies: 399 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):70,687,890-70,801,722Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6327085Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr170,222,20770,336,039
    nsv6327085RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr170,687,89070,801,722

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18204342duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18204342Submitted genomicNC_000001.11:g.702
    22207_70336039dup
    GRCh38 (hg38)NC_000001.11Chr170,222,20770,336,039
    nssv18204342RemappedPerfectNC_000001.10:g.706
    87890_70801722dup
    GRCh37.p13First PassNC_000001.10Chr170,687,89070,801,722

    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)
    nssv18204342<0.001139260
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