A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4437e59



Internal ID22765657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68220553..68226814hg38UCSC Ensembl
chr9:70835469..70841730hg19UCSC Ensembl
chr9:70025252..70031550hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg386262
hg196262
hg186299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3366092, esv3366297, esv3443800, esv3442046
SamplesNA12891, NA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4437e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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