A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1132e59



Internal ID20127881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113446336..113447734hg38UCSC Ensembl
chr13:114100651..114102049hg19UCSC Ensembl
chr13:113148652..113150050hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3367356, esv3355770
SamplesNA19239, NA19240
Known GenesADPRHL1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1132e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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