A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556730



Internal ID18757806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2674307..2675940hg38UCSC Ensembl
Outerchr20:2674294..2675976hg38UCSC Ensembl
Innerchr20:2654953..2656586hg19UCSC Ensembl
Outerchr20:2654940..2656622hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381683
hg191683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755477
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556730
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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