A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4882n54



Internal ID22772777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4315338..4316720hg38UCSC Ensembl
chr16:4365339..4366721hg19UCSC Ensembl
chr16:4305340..4306722hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381383
hg191383
hg181383
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571290, nsv571286
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4882n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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