A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1133e59



Internal ID22762353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113613136..113614734hg38UCSC Ensembl
chr13:114267451..114269049hg19UCSC Ensembl
chr13:113315452..113317050hg18UCSC 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 Variantsesv3414728, esv3451053
SamplesNA19239, NA19240
Known GenesTFDP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1133e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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