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nsv7082312

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:606

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 255 SVs from 18 studies. See in: genome view    
    Submitted genomic110,331,682-110,332,287Question Mark
    Overlapping variant regions from other studies: 255 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):109,574,910-109,575,515Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7082312Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX110,331,682110,332,287
    nsv7082312RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX109,574,910109,575,515

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18454417deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18454417Submitted genomicNC_000023.11:g.110
    331682_110332287de
    l
    GRCh38 (hg38)NC_000023.11ChrX110,331,682110,332,287
    nssv18454417RemappedPerfectNC_000023.10:g.109
    574910_109575515de
    l
    GRCh37.p13First PassNC_000023.10ChrX109,574,910109,575,515

    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)
    nssv184544175e-061200000
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