A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1878e59



Internal ID22763098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35931291..35931589hg38UCSC Ensembl
chr18:33511254..33511552hg19UCSC Ensembl
chr18:31765252..31765550hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38299
hg19299
hg18299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3352988, esv3392629
SamplesNA19238, NA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1878e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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