A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999373



Internal ID7064892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196828364..196830482hg38UCSC Ensembl
Innerchr3:196555235..196557353hg19UCSC Ensembl
Innerchr3:198039632..198041750hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382119
hg192119
hg182119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586279
SamplesHuRef
Known GenesPAK2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999373
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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