A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8169n54



Internal ID20141593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2478019..2551860hg38UCSC Ensembl
chr3:2519703..2593544hg19UCSC Ensembl
chr3:2494703..2568544hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3873842
hg1973842
hg1873842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589386, nsv589387
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8169n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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