A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1626e59



Internal ID22762846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70150848..70153846hg38UCSC Ensembl
chr16:70184751..70187749hg19UCSC Ensembl
chr16:68742252..68745250hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382999
hg192999
hg182999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3384528, esv3352116, esv3348468
SamplesNA19239, NA12892, NA19240
Known GenesPDPR
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1626e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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