A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678156



Internal ID9944261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58140749..58142495hg38UCSC Ensembl
Outerchr20:58140712..58142545hg38UCSC Ensembl
Innerchr20:56715805..56717551hg19UCSC Ensembl
Outerchr20:56715768..56717601hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381834
hg191834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6220780
SamplesNA19438
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678156
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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