A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4883n54



Internal ID22772778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4315338..4316990hg38UCSC Ensembl
chr16:4365339..4366991hg19UCSC Ensembl
chr16:4305340..4306992hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381653
hg191653
hg181653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571285, nsv571294, nsv571284, nsv571292, nsv571291
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4883n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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