A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv883e214



Internal ID22756777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34419757..34589742hg38UCSC Ensembl
chr3:34461249..34631234hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38169986
hg19169986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595814, esv3595812
SamplesNA19066, HG02262, HG01486, NA18988, HG01344
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv883e214
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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