A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11153436



Internal ID1155252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132226625..132270546hg38UCSC Ensembl
chr3:131945469..131989390hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3843922
hg1943922
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597818
Supporting Variants
SamplesNA19019
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11153436
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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