A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667966



Internal ID9587385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2096841..2098867hg38UCSC Ensembl
Outerchr20:2096804..2098917hg38UCSC Ensembl
Innerchr20:2077487..2079513hg19UCSC Ensembl
Outerchr20:2077450..2079563hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382114
hg192114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6148327
SamplesHG00740
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667966
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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