A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597884



Internal ID6985022
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11156816
SamplesHG03559
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597884
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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