A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1117e59



Internal ID22762337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111974337..111975935hg38UCSC Ensembl
chr13:112628651..112630249hg19UCSC Ensembl
chr13:111676652..111678250hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3360829, esv3355757, esv3381880
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1117e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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