A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11069217



Internal ID3262895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:90132522..90145302hg38UCSC Ensembl
chr3:90181672..90194452hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3812781
hg1912781
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596983
Supporting Variants
SamplesHG02882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11069217
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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