A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586486



Internal ID7057868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26905190..26908750hg38UCSC Ensembl
Innerchr22:27301153..27304713hg19UCSC Ensembl
Innerchr22:25631153..25634713hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg383561
hg193561
hg183561
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995430
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586486
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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