A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv706e59



Internal ID22761926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112253819..112255517hg38UCSC Ensembl
chr11:112124542..112126240hg19UCSC Ensembl
chr11:111629752..111631450hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3334996, esv3347284
SamplesNA19238, NA19240
Known GenesPLET1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv706e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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