A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668087



Internal ID9934192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34777999..34781160hg38UCSC Ensembl
Outerchr20:34777814..34781358hg38UCSC Ensembl
Innerchr20:33365802..33368963hg19UCSC Ensembl
Outerchr20:33365617..33369161hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383545
hg193545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6471573, essv6031820
SamplesNA19057, HG00512
Known GenesNCOA6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668087
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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