A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4438e59



Internal ID22765658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68237216..68249014hg38UCSC Ensembl
chr9:70852132..70863930hg19UCSC Ensembl
chr9:70041952..70053750hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3811799
hg1911799
hg1811799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3399368, esv3352562
SamplesNA12878, NA12892
Known GenesCBWD3, CBWD5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4438e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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