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nsv6775874

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,030

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 18 studies. See in: genome view    
    Submitted genomic124,067,157-124,068,186Question Mark
    Overlapping variant regions from other studies: 111 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):123,402,850-123,403,879Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6775874Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5124,067,157124,068,186
    nsv6775874RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5123,402,850123,403,879

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18693899duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18693899Submitted genomicNC_000005.10:g.124
    067157_124068186du
    p
    GRCh38 (hg38)NC_000005.10Chr5124,067,157124,068,186
    nssv18693899RemappedPerfectNC_000005.9:g.1234
    02850_123403879dup
    GRCh37.p13First PassNC_000005.9Chr5123,402,850123,403,879

    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)
    nssv186938994e-061262640
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