A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3263n100



Internal ID22789350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52417469..52508733hg38UCSC Ensembl
chr17:50494829..50586093hg19UCSC Ensembl
chr17:47849828..47941092hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3891265
hg1991265
hg1891265
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065519, nsv1060938
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3263n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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