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nsv7086116

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,966

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 285 SVs from 16 studies. See in: genome view    
    Submitted genomic19,932,680-19,935,645Question Mark
    Overlapping variant regions from other studies: 286 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):19,950,798-19,953,763Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086116Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX19,932,68019,935,645
    nsv7086116RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX19,950,79819,953,763

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18452532deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18452532Submitted genomicNC_000023.11:g.199
    32680_19935645del
    GRCh38 (hg38)NC_000023.11ChrX19,932,68019,935,645
    nssv18452532RemappedPerfectNC_000023.10:g.199
    50798_19953763del
    GRCh37.p13First PassNC_000023.10ChrX19,950,79819,953,763

    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)
    nssv184525329e-062222222
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