A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8167n54



Internal ID20141591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2452396..2454664hg38UCSC Ensembl
chr3:2494080..2496348hg19UCSC Ensembl
chr3:2469080..2471348hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg382269
hg192269
hg182269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589379, nsv589380
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8167n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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