A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661015



Internal ID9927120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52038162..52038995hg38UCSC Ensembl
chr20:50654701..50655534hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6114102, essv6061980, essv5608510, essv5550558, essv6098172, essv5712023, essv5509506, essv5873905, essv6057224, essv6424424, essv6000836, essv6062232, essv6378306, essv5918067
SamplesNA18924, NA19443, NA18923, NA18856, NA19469, NA19436, NA19375, NA19712, NA19470, NA19311, HG01137, NA19472, NA19316, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661015
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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