A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010803



Internal ID6722894
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586093
SamplesHuRef
Known GenesPDE9A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010803
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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