A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8296n54



Internal ID20141720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41859164..42073996hg38UCSC Ensembl
chr3:41900656..42115488hg19UCSC Ensembl
chr3:41875660..42090492hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38214833
hg19214833
hg18214833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590141, nsv590140
SamplesHGDP00905
Known GenesULK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8296n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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