A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556893



Internal ID18757969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17122806..17123127hg38UCSC Ensembl
Outerchr20:17122719..17123203hg38UCSC Ensembl
Innerchr20:17103451..17103772hg19UCSC Ensembl
Outerchr20:17103364..17103848hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755640
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556893
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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