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nsv6844338

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 216 SVs from 37 studies. See in: genome view    
    Submitted genomic133,153,701-133,168,300Question Mark
    Overlapping variant regions from other studies: 216 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):134,165,945-134,180,544Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6844338Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8133,153,701133,168,300
    nsv6844338RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8134,165,945134,180,544

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18551382deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18551382Submitted genomicNC_000008.11:g.133
    153701_133168300de
    l
    GRCh38 (hg38)NC_000008.11Chr8133,153,701133,168,300
    nssv18551382RemappedPerfectNC_000008.10:g.134
    165945_134180544de
    l
    GRCh37.p13First PassNC_000008.10Chr8134,165,945134,180,544

    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)
    nssv18551382<0.001228252660
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