A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv863e214



Internal ID20122286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4041939..4088910hg38UCSC Ensembl
chr3:4083623..4130594hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3846972
hg1946972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595079, esv3595078
SamplesNA19701, HG01305, NA20798, NA20903, HG04054, HG00254
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv863e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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