A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv727e59



Internal ID20127476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133901547..133902745hg38UCSC Ensembl
chr11:133771442..133772640hg19UCSC Ensembl
chr11:133276652..133277850hg18UCSC Ensembl
Cytoband11q25
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 Variantsesv3384459, esv3407372
SamplesNA19239, NA19240
Known GenesMIR4697HG
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv727e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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