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nsv6793509

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 23 studies. See in: genome view    
    Submitted genomic141,510,901-141,517,000Question Mark
    Overlapping variant regions from other studies: 87 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):140,890,468-140,896,567Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6793509Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5141,510,901141,517,000
    nsv6793509RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,890,468140,896,567

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18699154duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18699154Submitted genomicNC_000005.10:g.141
    510901_141517000du
    p
    GRCh38 (hg38)NC_000005.10Chr5141,510,901141,517,000
    nssv18699154RemappedPerfectNC_000005.9:g.1408
    90468_140896567dup
    GRCh37.p13First PassNC_000005.9Chr5140,890,468140,896,567

    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)
    nssv186991541.8e-055271118
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