A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663528



Internal ID9929633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65364648..65371860hg38UCSC Ensembl
Outerchr11:65364491..65372013hg38UCSC Ensembl
Innerchr11:65132119..65139331hg19UCSC Ensembl
Outerchr11:65131962..65139484hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387523
hg197523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6135409
SamplesHG00513
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663528
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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