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nsv7078275

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 263 SVs from 22 studies. See in: genome view    
    Submitted genomic107,270,201-107,274,100Question Mark
    Overlapping variant regions from other studies: 263 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):106,513,431-106,517,330Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7078275Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX107,270,201107,274,100
    nsv7078275RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX106,513,431106,517,330

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18653442duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18653442Submitted genomicNC_000023.11:g.107
    270201_107274100du
    p
    GRCh38 (hg38)NC_000023.11ChrX107,270,201107,274,100
    nssv18653442RemappedPerfectNC_000023.10:g.106
    513431_106517330du
    p
    GRCh37.p13First PassNC_000023.10ChrX106,513,431106,517,330

    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)
    nssv186534429e-062222222
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