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nsv7080473

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,860

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 387 SVs from 39 studies. See in: genome view    
    Submitted genomic22,978,853-23,023,712Question Mark
    Overlapping variant regions from other studies: 388 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):22,996,970-23,041,829Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7080473Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX22,978,85323,023,712
    nsv7080473RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX22,996,97023,041,829

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18657570duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18657570Submitted genomicNC_000023.11:g.229
    78853_23023712dup
    GRCh38 (hg38)NC_000023.11ChrX22,978,85323,023,712
    nssv18657570RemappedPerfectNC_000023.10:g.229
    96970_23041829dup
    GRCh37.p13First PassNC_000023.10ChrX22,996,97023,041,829

    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)
    nssv186575705e-061200000
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