A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1116e59



Internal ID22762336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111620304..111622202hg38UCSC Ensembl
chr13:112272651..112274549hg19UCSC Ensembl
chr13:111070652..111072550hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3354040, esv3392916
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1116e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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