A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1884e59



Internal ID22763104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39800890..39803288hg38UCSC Ensembl
chr18:37380854..37383252hg19UCSC Ensembl
chr18:35634852..35637250hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg382399
hg192399
hg182399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3358895, esv3393903
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1884e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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