A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564461



Internal ID18765537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:113617617..113617897hg38UCSC Ensembl
Outerchr4:113617585..113617918hg38UCSC Ensembl
Innerchr4:114538773..114539053hg19UCSC Ensembl
Outerchr4:114538741..114539074hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763208
Samples
Known GenesCAMK2D
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564461
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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