A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1129e59



Internal ID18986630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113111137..113113335hg38UCSC Ensembl
chr13:113765451..113767649hg19UCSC Ensembl
chr13:112813452..112815650hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382199
hg192199
hg182199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3376802, esv3417798
SamplesNA19239, NA12891
Known GenesF7
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1129e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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