A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596983



Internal ID6984297
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11069218, essv11069217
SamplesHG03926, HG02882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596983
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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