A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1114e59



Internal ID22762334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110873404..110874502hg38UCSC Ensembl
chr13:111525751..111526849hg19UCSC Ensembl
chr13:110323752..110324850hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3394634, esv3403043, esv3434793
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1114e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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