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nsv7014218

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,223

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 172 SVs from 28 studies. See in: genome view    
    Submitted genomic32,650,153-32,667,375Question Mark
    Overlapping variant regions from other studies: 172 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):33,141,059-33,158,281Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7014218Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1932,650,15332,667,375
    nsv7014218RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1933,141,05933,158,281

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18640112duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18640112Submitted genomicNC_000019.10:g.326
    50153_32667375dup
    GRCh38 (hg38)NC_000019.10Chr1932,650,15332,667,375
    nssv18640112RemappedPerfectNC_000019.9:g.3314
    1059_33158281dup
    GRCh37.p13First PassNC_000019.9Chr1933,141,05933,158,281

    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)
    nssv186401124e-061275984
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