A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1924e59



Internal ID22763144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75086008..75087406hg38UCSC Ensembl
chr18:72797964..72799362hg19UCSC Ensembl
chr18:70926952..70928350hg18UCSC Ensembl
Cytoband18q22.3
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 Variantsesv3388477, esv3360254
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1924e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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