A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675339



Internal ID9594758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111769289..111771666hg38UCSC Ensembl
Outerchr11:111769236..111771737hg38UCSC Ensembl
Innerchr11:111640013..111642390hg19UCSC Ensembl
Outerchr11:111639960..111642461hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6488825
SamplesHG01461
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675339
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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