A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4342e59



Internal ID22765562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65145877..65150876hg38UCSC Ensembl
chr9:42851256..42856254hg19UCSC Ensembl
chr9:42841252..42846250hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385000
hg194999
hg184999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3356257, esv3369915
SamplesNA12891, NA19240
Known GenesLOC286297
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4342e59
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