A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564800



Internal ID18765876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151869766..151873111hg38UCSC Ensembl
Outerchr4:151868849..151874333hg38UCSC Ensembl
Innerchr4:152790918..152794263hg19UCSC Ensembl
Outerchr4:152790001..152795485hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg385485
hg195485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763547
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564800
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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