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nsv7013247

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:232,241

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 845 SVs from 69 studies. See in: genome view    
    Submitted genomic5,408,898-5,641,138Question Mark
    Overlapping variant regions from other studies: 845 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):5,389,544-5,621,784Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7013247Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr205,408,8985,641,138
    nsv7013247RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr205,389,5445,621,784

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644367duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644367Submitted genomicNC_000020.11:g.540
    8898_5641138dup
    GRCh38 (hg38)NC_000020.11Chr205,408,8985,641,138
    nssv18644367RemappedPerfectNC_000020.10:g.538
    9544_5621784dup
    GRCh37.p13First PassNC_000020.10Chr205,389,5445,621,784

    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)
    nssv186443671.8e-055275430
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