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nsv7092466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:197

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 230 SVs from 21 studies. See in: genome view    
    Submitted genomic73,989,249-73,989,445Question Mark
    Overlapping variant regions from other studies: 230 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):73,209,084-73,209,280Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7092466Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX73,989,24973,989,445
    nsv7092466RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX73,209,08473,209,280

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18660675duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18660675Submitted genomicNC_000023.11:g.739
    89249_73989445dup
    GRCh38 (hg38)NC_000023.11ChrX73,989,24973,989,445
    nssv18660675RemappedPerfectNC_000023.10:g.732
    09084_73209280dup
    GRCh37.p13First PassNC_000023.10ChrX73,209,08473,209,280

    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)
    nssv186606755e-061200000
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