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nsv7086122

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:137

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 276 SVs from 16 studies. See in: genome view    
    Submitted genomic19,958,541-19,958,677Question Mark
    Overlapping variant regions from other studies: 277 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):19,976,659-19,976,795Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086122Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX19,958,54119,958,677
    nsv7086122RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX19,976,65919,976,795

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655116duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655116Submitted genomicNC_000023.11:g.199
    58541_19958677dup
    GRCh38 (hg38)NC_000023.11ChrX19,958,54119,958,677
    nssv18655116RemappedPerfectNC_000023.10:g.199
    76659_19976795dup
    GRCh37.p13First PassNC_000023.10ChrX19,976,65919,976,795

    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)
    nssv186551169e-062222222
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