A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1211e59



Internal ID22762431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21581577..21590891hg38UCSC Ensembl
chr14:22049712..22059010hg19UCSC Ensembl
chr14:21119552..21128850hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg389315
hg199299
hg189299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3343885, esv3443599, esv3440788, esv3374503
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1211e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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