A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671239



Internal ID9590658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65805817..65812907hg38UCSC Ensembl
chr11:65573288..65580378hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387091
hg197091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5668673, essv5817504, essv5936127, essv6304257, essv6547433, essv6157995, essv6250404
SamplesNA18868, NA19347, HG01095, NA19395, NA19835, NA19311, NA19213
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671239
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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