A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4353e59



Internal ID22765573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64399966..64407757hg38UCSC Ensembl
chr9:43095356..43103154hg19UCSC Ensembl
chr9:43085352..43093150hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg387792
hg197799
hg187799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3385868, esv3447918
SamplesNA12878, NA12892
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4353e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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