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nsv6333218

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 86 SVs from 20 studies. See in: genome view    
    Submitted genomic32,319,801-32,320,900Question Mark
    Overlapping variant regions from other studies: 86 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):32,785,402-32,786,501Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6333218Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr132,319,80132,320,900
    nsv6333218RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr132,785,40232,786,501

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18060446deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18060446Submitted genomicNC_000001.11:g.323
    19801_32320900del
    GRCh38 (hg38)NC_000001.11Chr132,319,80132,320,900
    nssv18060446RemappedPerfectNC_000001.10:g.327
    85402_32786501del
    GRCh37.p13First PassNC_000001.10Chr132,785,40232,786,501

    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)
    nssv18060446<0.001136042
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