A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1522e59



Internal ID22762742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32167030..32176128hg38UCSC Ensembl
chr16:32178351..32187449hg19UCSC Ensembl
chr16:32085852..32094950hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg389099
hg199099
hg189099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3400647, esv3392228, esv3408261
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1522e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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