A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666225



Internal ID9585644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34554449..34555914hg38UCSC Ensembl
Outerchr20:34554412..34555964hg38UCSC Ensembl
Innerchr20:33142253..33143718hg19UCSC Ensembl
Outerchr20:33142216..33143768hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381553
hg191553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5899138
SamplesHG00734
Known GenesMAP1LC3A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666225
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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