A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664599



Internal ID9930704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33458639..33460140hg38UCSC Ensembl
Outerchr20:33458482..33460293hg38UCSC Ensembl
Innerchr20:32046445..32047946hg19UCSC Ensembl
Outerchr20:32046288..32048099hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5929556
SamplesNA19462
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664599
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer