A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1196e59



Internal ID22762416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19750353..19776951hg38UCSC Ensembl
chr14:20218512..20245110hg19UCSC Ensembl
chr14:19288352..19314950hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3826599
hg1926599
hg1826599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3407444, esv3349928
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1196e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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