A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586546



Internal ID7057928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22448196..22518136hg38UCSC Ensembl
Innerchr14:22917188..22987114hg19UCSC Ensembl
Innerchr14:21987028..22056954hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3869941
hg1969927
hg1869927
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992622
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586546
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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