A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11026587



Internal ID3480809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62956283..63091452hg38UCSC Ensembl
chr3:62941958..63077128hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38135170
hg19135171
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596381
Supporting Variants
SamplesHG03096
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11026587
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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