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nsv7086024

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,370

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 309 SVs from 26 studies. See in: genome view    
    Submitted genomic18,964,313-18,974,682Question Mark
    Overlapping variant regions from other studies: 310 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):18,982,431-18,992,800Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086024Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX18,964,31318,974,682
    nsv7086024RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX18,982,43118,992,800

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18459125deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18459125Submitted genomicNC_000023.11:g.189
    64313_18974682del
    GRCh38 (hg38)NC_000023.11ChrX18,964,31318,974,682
    nssv18459125RemappedPerfectNC_000023.10:g.189
    82431_18992800del
    GRCh37.p13First PassNC_000023.10ChrX18,982,43118,992,800

    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)
    nssv184591255e-061200000
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