nsv4296187

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52,137,762

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93553 SVs from 126 studies. See in: genome view    
    Remapped(Score: Good):37,348,877-89,486,638Question Mark
    Overlapping variant regions from other studies: 93753 SVs from 126 studies. See in: genome view    
    Submitted genomic37,370,427-89,219,806Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv4296187RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1137,348,87789,486,638
    nsv4296187Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1137,370,42789,219,806

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15496874insertionSequencingOther

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv15496874RemappedGoodNC_000011.10:g.373
    48877_89486638ins7
    6
    GRCh38.p12First PassNC_000011.10Chr1137,348,87789,486,638
    nssv15496874Submitted genomicNC_000011.9:g.3737
    0427_89219806ins76
    GRCh37.p13NC_000011.9Chr1137,370,42789,219,806

    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)
    nssv154968740.106216620400
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