A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663913



Internal ID9930018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16226510..16228464hg38UCSC Ensembl
chr20:16207155..16209109hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381955
hg191955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5773331, essv5885222, essv5840075, essv5913526, essv5556944, essv5654285, essv6590888, essv6057106, essv5692813
SamplesNA19700, NA18504, NA19198, NA20317, NA18498, NA20344, NA19434, NA19439, NA19438
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663913
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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