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nsv7091316

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:750,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1103 SVs from 59 studies. See in: genome view    
    Submitted genomic26,008,601-26,759,000Question Mark
    Overlapping variant regions from other studies: 1104 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):26,026,718-26,777,117Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7091316Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX26,008,60126,759,000
    nsv7091316RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX26,026,71826,777,117

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655278duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655278Submitted genomicNC_000023.11:g.260
    08601_26759000dup
    GRCh38 (hg38)NC_000023.11ChrX26,008,60126,759,000
    nssv18655278RemappedPerfectNC_000023.10:g.260
    26718_26777117dup
    GRCh37.p13First PassNC_000023.10ChrX26,026,71826,777,117

    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)
    nssv186552785e-061200000
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