A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557028



Internal ID18411418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35128254..35128836hg38UCSC Ensembl
Outerchr20:35128123..35129037hg38UCSC Ensembl
Innerchr20:33716057..33716639hg19UCSC Ensembl
Outerchr20:33715926..33716840hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755775
Samples
Known GenesEDEM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557028
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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