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nsv6791711

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,432

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 26 studies. See in: genome view    
    Submitted genomic149,626,370-149,640,801Question Mark
    Overlapping variant regions from other studies: 118 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):149,005,933-149,020,364Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6791711Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5149,626,370149,640,801
    nsv6791711RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5149,005,933149,020,364

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18695629duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18695629Submitted genomicNC_000005.10:g.149
    626370_149640801du
    p
    GRCh38 (hg38)NC_000005.10Chr5149,626,370149,640,801
    nssv18695629RemappedPerfectNC_000005.9:g.1490
    05933_149020364dup
    GRCh37.p13First PassNC_000005.9Chr5149,005,933149,020,364

    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)
    nssv186956296.4e-0518274312
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