U.S. flag

An official website of the United States government

nsv7086023

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:290

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 293 SVs from 19 studies. See in: genome view    
    Submitted genomic18,963,651-18,963,940Question Mark
    Overlapping variant regions from other studies: 294 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):18,981,769-18,982,058Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086023Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX18,963,65118,963,940
    nsv7086023RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX18,981,76918,982,058

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18656630duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18656630Submitted genomicNC_000023.11:g.189
    63651_18963940dup
    GRCh38 (hg38)NC_000023.11ChrX18,963,65118,963,940
    nssv18656630RemappedPerfectNC_000023.10:g.189
    81769_18982058dup
    GRCh37.p13First PassNC_000023.10ChrX18,981,76918,982,058

    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)
    nssv186566305e-061200000
    Support Center