A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv531n21



Internal ID20132252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135533826..135691851hg38UCSC Ensembl
chrX:134667751..134825566hg19UCSC Ensembl
chrX:134495417..134653232hg18UCSC Ensembl
chrX:134393271..134551086hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38158026
hg19157816
hg18157816
hg17157816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523594, nsv519163
Samples
Known GenesDDX26B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv531n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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