A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2399e59



Internal ID22763619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11368804..11370002hg38UCSC Ensembl
chr20:11349452..11350650hg19UCSC Ensembl
chr20:11297452..11298650hg18UCSC Ensembl
Cytoband20p12.2
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 Variantsesv3432469, esv3388930, esv3376008
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2399e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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