A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755652



Internal ID18729898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:18197399..18198514hg38UCSC Ensembl
Outerchr20:18197339..18198702hg38UCSC Ensembl
Innerchr20:18178043..18179158hg19UCSC Ensembl
Outerchr20:18177983..18179346hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755652
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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