A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4398e59



Internal ID22765618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63303460..63314158hg38UCSC Ensembl
chr9:67258432..67269130hg19UCSC Ensembl
chr9:66948252..66958950hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3810699
hg1910699
hg1810699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3385755, esv3417649, esv3384405, esv3428956
SamplesNA12891, NA19239, NA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4398e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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