A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11156816



Internal ID3905697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136223968..136239803hg38UCSC Ensembl
chr3:135942810..135958645hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3815836
hg1915836
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597884
Supporting Variants
SamplesHG03559
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11156816
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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