A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557139



Internal ID18758215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47390331..47390642hg38UCSC Ensembl
Outerchr20:47390272..47390719hg38UCSC Ensembl
Innerchr20:46019075..46019386hg19UCSC Ensembl
Outerchr20:46019016..46019463hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755886
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557139
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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