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nsv6550126

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,615

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 20 studies. See in: genome view    
    Submitted genomic34,781,854-34,783,468Question Mark
    Overlapping variant regions from other studies: 147 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):36,154,151-36,155,765Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6550126Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2134,781,85434,783,468
    nsv6550126RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2136,154,15136,155,765

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18072116deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18072116Submitted genomicNC_000021.9:g.3478
    1854_34783468del
    GRCh38 (hg38)NC_000021.9Chr2134,781,85434,783,468
    nssv18072116RemappedPerfectNC_000021.8:g.3615
    4151_36155765del
    GRCh37.p13First PassNC_000021.8Chr2136,154,15136,155,765

    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)
    nssv18072116<0.001138422
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