A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv542e59



Internal ID20127291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:530452..531450hg38UCSC Ensembl
chr11:530452..531450hg19UCSC Ensembl
chr11:520452..521450hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3432176, esv3443089
SamplesNA12891, NA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv542e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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