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nsv7085992

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:89,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 421 SVs from 36 studies. See in: genome view    
    Submitted genomic18,606,901-18,696,400Question Mark
    Overlapping variant regions from other studies: 422 SVs from 36 studies. See in: genome view    
    Remapped(Score: Good):18,625,021-18,714,519Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7085992Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX18,606,90118,696,400
    nsv7085992RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX18,625,02118,714,519

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18656609duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18656609Submitted genomicNC_000023.11:g.186
    06901_18696400dup
    GRCh38 (hg38)NC_000023.11ChrX18,606,90118,696,400
    nssv18656609RemappedGoodNC_000023.10:g.186
    25021_18714519dup
    GRCh37.p13First PassNC_000023.10ChrX18,625,02118,714,519

    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)
    nssv186566095e-061200000
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