A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4963n54



Internal ID20138387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27329738..27340800hg38UCSC Ensembl
chr16:27341059..27352121hg19UCSC Ensembl
chr16:27248560..27259622hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3811063
hg1911063
hg1811063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571716, nsv571718, nsv571717, nsv571719, nsv571715, nsv571720
Samples
Known GenesIL4R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4963n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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