A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761823



Internal ID18736069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190237653..190237882hg38UCSC Ensembl
Outerchr3:190237598..190237943hg38UCSC Ensembl
Innerchr3:189955442..189955671hg19UCSC Ensembl
Outerchr3:189955387..189955732hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761823
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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