A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4429e59



Internal ID20131178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65659644..65678513hg38UCSC Ensembl
chr9:70487532..70506430hg19UCSC Ensembl
chr9:69727352..69746250hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3818870
hg1918899
hg1818899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3442658, esv3449709
SamplesNA12878, NA12892
Known GenesCBWD3, CBWD5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4429e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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