A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563326



Internal ID18764402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6420274..6421778hg38UCSC Ensembl
Outerchr4:6420245..6421789hg38UCSC Ensembl
Innerchr4:6422001..6423505hg19UCSC Ensembl
Outerchr4:6421972..6423516hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381545
hg191545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762073
Samples
Known GenesPPP2R2C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563326
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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