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nsv7088444

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,439

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 290 SVs from 32 studies. See in: genome view    
    Submitted genomic68,703,129-68,768,567Question Mark
    Overlapping variant regions from other studies: 292 SVs from 33 studies. See in: genome view    
    Remapped(Score: Good):67,922,971-67,988,410Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7088444Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX68,703,12968,768,567
    nsv7088444RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX67,922,97167,988,410

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659056duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659056Submitted genomicNC_000023.11:g.687
    03129_68768567dup
    GRCh38 (hg38)NC_000023.11ChrX68,703,12968,768,567
    nssv18659056RemappedGoodNC_000023.10:g.679
    22971_67988410dup
    GRCh37.p13First PassNC_000023.10ChrX67,922,97167,988,410

    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)
    nssv186590563.7e-058216216
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