A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5765106



Internal ID8955791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34159257..34160298hg38UCSC Ensembl
Outerchr20:34159220..34160348hg38UCSC Ensembl
Innerchr20:32747063..32748104hg19UCSC Ensembl
Outerchr20:32747026..32748154hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666238
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5765106
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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