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nsv7092385

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:349,071

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 655 SVs from 55 studies. See in: genome view    
    Submitted genomic73,568,179-73,917,249Question Mark
    Overlapping variant regions from other studies: 655 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):72,788,015-73,137,084Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7092385Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX73,568,17973,917,249
    nsv7092385RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX72,788,01573,137,084

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659877duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659877Submitted genomicNC_000023.11:g.735
    68179_73917249dup
    GRCh38 (hg38)NC_000023.11ChrX73,568,17973,917,249
    nssv18659877RemappedPerfectNC_000023.10:g.727
    88015_73137084dup
    GRCh37.p13First PassNC_000023.10ChrX72,788,01573,137,084

    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)
    nssv186598775e-061200000
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