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nsv7017906

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,328

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 170 SVs from 39 studies. See in: genome view    
    Submitted genomic51,339,840-51,354,167Question Mark
    Overlapping variant regions from other studies: 170 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):51,843,094-51,857,421Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017906Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1951,339,84051,354,167
    nsv7017906RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1951,843,09451,857,421

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638741duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638741Submitted genomicNC_000019.10:g.513
    39840_51354167dup
    GRCh38 (hg38)NC_000019.10Chr1951,339,84051,354,167
    nssv18638741RemappedPerfectNC_000019.9:g.5184
    3094_51857421dup
    GRCh37.p13First PassNC_000019.9Chr1951,843,09451,857,421

    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)
    nssv186387414e-061276028
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