A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1206e59



Internal ID22762426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19913453..19942651hg38UCSC Ensembl
chr14:20381612..20410810hg19UCSC Ensembl
chr14:19451452..19480650hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3829199
hg1929199
hg1829199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3380814, esv3362518
SamplesNA19239, NA19240
Known GenesOR4K1, OR4K5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1206e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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