A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv552e59



Internal ID22761772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2433546..2434844hg38UCSC Ensembl
chr11:2454776..2456074hg19UCSC Ensembl
chr11:2411352..2412650hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3359791, esv3402475
SamplesNA19238, NA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv552e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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