A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5929556



Internal ID9709258
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 Flag1
Merged StatusS
Merged Variantsesv2664599
Supporting Variants
SamplesNA19462
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5929556
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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