A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1137e59



Internal ID22762357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113983839..113990972hg38UCSC Ensembl
chr13:114753250..114756448hg19UCSC Ensembl
chr13:113771352..113774550hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg387134
hg193199
hg183199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3333473, esv3428321
SamplesNA19239, NA19240
Known GenesRASA3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1137e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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