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nsv7055654

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,889

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 259 SVs from 20 studies. See in: genome view    
    Submitted genomic110,384,816-110,389,704Question Mark
    Overlapping variant regions from other studies: 259 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):109,628,044-109,632,932Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055654Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX110,384,816110,389,704
    nsv7055654RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX109,628,044109,632,932

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765698inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765698Submitted genomicNC_000023.11:g.110
    384816_110389704in
    v
    GRCh38 (hg38)NC_000023.11ChrX110,384,816110,389,704
    nssv18765698RemappedPerfectNC_000023.10:g.109
    628044_109632932in
    v
    GRCh37.p13First PassNC_000023.10ChrX109,628,044109,632,932

    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)
    nssv187656985e-061200000
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