A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664908



Internal ID9931013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18052720..18054590hg38UCSC Ensembl
chr11:18074267..18076137hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381871
hg191871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6484483
SamplesNA18541
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664908
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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