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nsv7080537

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 296 SVs from 23 studies. See in: genome view    
    Submitted genomic23,256,501-23,266,000Question Mark
    Overlapping variant regions from other studies: 297 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):23,274,618-23,284,117Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7080537Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX23,256,50123,266,000
    nsv7080537RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX23,274,61823,284,117

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655169duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655169Submitted genomicNC_000023.11:g.232
    56501_23266000dup
    GRCh38 (hg38)NC_000023.11ChrX23,256,50123,266,000
    nssv18655169RemappedPerfectNC_000023.10:g.232
    74618_23284117dup
    GRCh37.p13First PassNC_000023.10ChrX23,274,61823,284,117

    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)
    nssv186551695e-061200000
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