A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5712668



Internal ID9113372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21022067..21022415hg38UCSC Ensembl
chr20:21002708..21003056hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675090
Supporting Variants
SamplesHG01111
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5712668
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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