A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6483522



Internal ID9436107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33586741..33597475hg38UCSC Ensembl
Outerchr20:33586584..33597628hg38UCSC Ensembl
Innerchr20:32174547..32185281hg19UCSC Ensembl
Outerchr20:32174390..32185434hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3811045
hg1911045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672530
Supporting Variants
SamplesNA18636
Known GenesCBFA2T2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6483522
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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