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nsv7010036

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:727

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 156 SVs from 18 studies. See in: genome view    
    Submitted genomic26,934,806-26,935,532Question Mark
    Overlapping variant regions from other studies: 156 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):24,514,770-24,515,496Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7010036Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1826,934,80626,935,532
    nsv7010036RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1824,514,77024,515,496

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18633280duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18633280Submitted genomicNC_000018.10:g.269
    34806_26935532dup
    GRCh38 (hg38)NC_000018.10Chr1826,934,80626,935,532
    nssv18633280RemappedPerfectNC_000018.9:g.2451
    4770_24515496dup
    GRCh37.p13First PassNC_000018.9Chr1824,514,77024,515,496

    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)
    nssv186332808e-062253940
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