A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674266



Internal ID9940371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45755471..45756339hg38UCSC Ensembl
Outerchr11:45755434..45756389hg38UCSC Ensembl
Innerchr11:45777022..45777890hg19UCSC Ensembl
Outerchr11:45776985..45777940hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5731710
SamplesNA19438
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674266
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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