A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4533e59



Internal ID22765753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133495209..133496807hg38UCSC Ensembl
chr9:136360331..136361929hg19UCSC Ensembl
chr9:135350152..135351750hg18UCSC Ensembl
Cytoband9q34.2
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 Variantsesv3445467, esv3380362
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4533e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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