A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv859e214



Internal ID20122282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2196255..2603583hg38UCSC Ensembl
chr3:2237939..2645267hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38407329
hg19407329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595021, esv3595018
SamplesHG04002, NA18592
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv859e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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