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nsv7088421

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:259,244

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 575 SVs from 50 studies. See in: genome view    
    Submitted genomic68,502,071-68,761,314Question Mark
    Overlapping variant regions from other studies: 575 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):67,721,913-67,981,156Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7088421Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX68,502,07168,761,314
    nsv7088421RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX67,721,91367,981,156

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659045duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659045Submitted genomicNC_000023.11:g.685
    02071_68761314dup
    GRCh38 (hg38)NC_000023.11ChrX68,502,07168,761,314
    nssv18659045RemappedPerfectNC_000023.10:g.677
    21913_67981156dup
    GRCh37.p13First PassNC_000023.10ChrX67,721,91367,981,156

    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)
    nssv186590455e-061200000
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