A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv555e59



Internal ID22761775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3653646..3655044hg38UCSC Ensembl
chr11:3674876..3676274hg19UCSC Ensembl
chr11:3631452..3632850hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3362096, esv3353668, esv3332707, esv3446921, esv3393517, esv3398560
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known GenesART1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv555e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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