A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665871



Internal ID9931976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21828269..21829244hg38UCSC Ensembl
chr20:21808907..21809882hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5613008, essv6316400
SamplesNA18909, NA19102
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665871
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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