A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv541e59



Internal ID20127290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:519152..520350hg38UCSC Ensembl
chr11:519152..520350hg19UCSC Ensembl
chr11:509152..510350hg18UCSC Ensembl
Cytoband11p15.5
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 Variantsesv3375296, esv3334330, esv3337691, esv3442499
SamplesNA12891, NA19238, NA19239, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv541e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer