A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1136e59



Internal ID20127885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113794820..113796718hg38UCSC Ensembl
chr13:114497793..114499691hg19UCSC Ensembl
chr13:113614252..113616150hg18UCSC 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 Variantsesv3366973, esv3365886
SamplesNA19239, NA19240
Known GenesTMEM255B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1136e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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