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nsv7088926

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:442,889

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 702 SVs from 60 studies. See in: genome view    
    Submitted genomic75,677,512-76,120,400Question Mark
    Overlapping variant regions from other studies: 515 SVs from 48 studies. See in: genome view    
    Remapped(Score: Pass):74,897,347-75,200,415Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7088926Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX75,677,51276,120,400
    nsv7088926RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX74,897,34775,200,415

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659334duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659334Submitted genomicNC_000023.11:g.756
    77512_76120400dup
    GRCh38 (hg38)NC_000023.11ChrX75,677,51276,120,400
    nssv18659334RemappedPassNC_000023.10:g.748
    97347_75200415dup
    GRCh37.p13First PassNC_000023.10ChrX74,897,34775,200,415

    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)
    nssv186593345e-061200000
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