A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2014e59



Internal ID20128763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41229507..41231105hg38UCSC Ensembl
chr19:41735412..41737010hg19UCSC Ensembl
chr19:46427252..46428850hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3452160, esv3353863
SamplesNA19239, NA19240
Known GenesAXL
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2014e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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