A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663190



Internal ID9929295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53712892..53716966hg38UCSC Ensembl
Outerchr20:53712733..53717165hg38UCSC Ensembl
Innerchr20:52329431..52333505hg19UCSC Ensembl
Outerchr20:52329272..52333704hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384433
hg194433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5882688
SamplesHG00650
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663190
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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