A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4378e59



Internal ID22765598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62563855..62584453hg38UCSC Ensembl
chr9:46875156..46895754hg19UCSC Ensembl
chr9:46715152..46735750hg18UCSC Ensembl
Cytoband9p11.1
Allele length
AssemblyAllele length
hg3820599
hg1920599
hg1820599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3432124, esv3348492
SamplesNA12891, NA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4378e59
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