A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586855



Internal ID7058237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32635992..32658226hg38UCSC Ensembl
Innerchr6:32603769..32626003hg19UCSC Ensembl
Innerchr6:32711747..32733981hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3822235
hg1922235
hg1822235
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998922
Supporting Variants
SamplesHuRef
Known GenesHLA-DQA1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586855
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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