A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586093



Internal ID6710789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42715023..42719341hg38UCSC Ensembl
Innerchr21:44135133..44139451hg19UCSC Ensembl
Innerchr21:43008202..43012520hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384319
hg194319
hg184319
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1010803
Supporting Variants
SamplesHuRef
Known GenesPDE9A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586093
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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