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nsv6905915

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,444

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 37 studies. See in: genome view    
    Submitted genomic61,787,251-61,820,694Question Mark
    Overlapping variant regions from other studies: 110 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):61,554,723-61,588,166Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6905915Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1161,787,25161,820,694
    nsv6905915RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1161,554,72361,588,166

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18575104duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18575104Submitted genomicNC_000011.10:g.617
    87251_61820694dup
    GRCh38 (hg38)NC_000011.10Chr1161,787,25161,820,694
    nssv18575104RemappedPerfectNC_000011.9:g.6155
    4723_61588166dup
    GRCh37.p13First PassNC_000011.9Chr1161,554,72361,588,166

    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)
    nssv185751047e-062275926
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