nsv4020369

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,115,540

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 157197 SVs from 130 studies. See in: genome view    
    Remapped(Score: Good):20,609,571-106,725,110Question Mark
    Overlapping variant regions from other studies: 157410 SVs from 130 studies. See in: genome view    
    Submitted genomic20,631,117-106,595,836Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv4020369RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1120,609,571106,725,110
    nsv4020369Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1120,631,117106,595,836

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15496657alu insertionSequencingOther

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv15496657RemappedGoodNC_000011.10:g.206
    09571_106725110ins
    281
    GRCh38.p12First PassNC_000011.10Chr1120,609,571106,725,110
    nssv15496657Submitted genomicNC_000011.9:g.2063
    1117_106595836ins2
    81
    GRCh37.p13NC_000011.9Chr1120,631,117106,595,836

    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)
    nssv15496657<0.001321476
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