A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv659e59



Internal ID18986160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65834005..65835203hg38UCSC Ensembl
chr11:65601476..65602674hg19UCSC Ensembl
chr11:65358052..65359250hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3364341, esv3328198
SamplesNA19238, NA19240
Known GenesSNX32
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv659e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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