A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586479



Internal ID6711175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70122534..70175775hg38UCSC Ensembl
Innerchr16:70156437..70209678hg19UCSC Ensembl
Innerchr16:68713938..68767179hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3853242
hg1953242
hg1853242
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007882
Supporting Variants
SamplesHuRef
Known GenesCLEC18C, PDPR
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586479
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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