A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586054



Internal ID7057436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32632814..32689745hg38UCSC Ensembl
Innerchr6:32600591..32657522hg19UCSC Ensembl
Innerchr6:32708569..32765500hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3856932
hg1956932
hg1856932
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003385
Supporting Variants
SamplesHuRef
Known GenesHLA-DQA1, HLA-DQB1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586054
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