A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586378



Internal ID7057760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:107973051..108023246hg38UCSC Ensembl
Innerchr3:107691898..107742093hg19UCSC Ensembl
Innerchr3:109174588..109224783hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3850196
hg1950196
hg1850196
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006663
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586378
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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