A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667835



Internal ID9933940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23726897..23802711hg38UCSC Ensembl
chr20:23707534..23783348hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3875815
hg1975815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5566400, essv5684242, essv5708128, essv5612254
SamplesHG00699, NA19002, NA19759, HG01491
Known GenesCST1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667835
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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