A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv284n97



Internal ID22815681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26641135..26675087hg38UCSC Ensembl
chr8:26498651..26532604hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3833953
hg1933954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154332, nsv1154333
Samples
Known GenesDPYSL2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv284n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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