A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4881n54



Internal ID22772776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4315234..4317220hg38UCSC Ensembl
chr16:4365235..4367221hg19UCSC Ensembl
chr16:4305236..4307222hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381987
hg191987
hg181987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571298, nsv571279, nsv571295, nsv571288, nsv571289, nsv571280, nsv571278, nsv571293
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4881n54
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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