A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659567



Internal ID9925672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8020897..8022844hg38UCSC Ensembl
chr20:8001544..8003491hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg381948
hg191948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5566308, essv5594138
SamplesNA18634, NA18577
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659567
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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