A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616569



Internal ID7003455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20343386..20418319hg38UCSC Ensembl
chr8:20200897..20275830hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3874934
hg1974934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13132511, essv13132510
SamplesNA20774, NA19401
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616569
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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