A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586219



Internal ID7057601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29943289..29970130hg38UCSC Ensembl
Innerchr6:29911066..29937907hg19UCSC Ensembl
Innerchr6:30019045..30045886hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3826842
hg1926842
hg1826842
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994074
Supporting Variants
SamplesHuRef
Known GenesHLA-A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586219
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