A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677639



Internal ID9943744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33258977..33264302hg38UCSC Ensembl
Outerchr11:33258940..33264352hg38UCSC Ensembl
Innerchr11:33280523..33285848hg19UCSC Ensembl
Outerchr11:33280486..33285898hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385413
hg195413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5990000
SamplesNA19063
Known GenesHIPK3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677639
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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