A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2007e59



Internal ID18987508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30434405..30435703hg38UCSC Ensembl
chr19:30925312..30926610hg19UCSC Ensembl
chr19:35617152..35618450hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3418896, esv3439901
SamplesNA19239, NA19240
Known GenesZNF536
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2007e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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