A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586235



Internal ID6710931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14688264..14708699hg38UCSC Ensembl
Innerchr16:14782121..14802556hg19UCSC Ensembl
Innerchr16:14689622..14710057hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3820436
hg1920436
hg1820436
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008243
Supporting Variants
SamplesHuRef
Known GenesPLA2G10
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586235
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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