A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5466283



Internal ID8443686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36533220..36534268hg38UCSC Ensembl
chr20:35161623..35162671hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658049
Supporting Variants
SamplesNA18505
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5466283
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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