A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8170n54



Internal ID20141594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2526528..2628024hg38UCSC Ensembl
chr3:2568212..2669708hg19UCSC Ensembl
chr3:2543212..2644708hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38101497
hg19101497
hg18101497
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589389, nsv589390
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8170n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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