A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1139e59



Internal ID22762359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:18223524..18281473hg38UCSC Ensembl
chr14:19000001..19057950hg19UCSC Ensembl
chr14:18069952..18127950hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg3857950
hg1957950
hg1857999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3409051, esv3381218, esv3374078, esv3376720, esv3447787
SamplesNA12891, NA19238, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1139e59
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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