A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4397e59



Internal ID22765617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63295860..63301958hg38UCSC Ensembl
chr9:67250832..67256930hg19UCSC Ensembl
chr9:66940652..66946750hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg386099
hg196099
hg186099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3350873, esv3399983
SamplesNA19239, NA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4397e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer