A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659576



Internal ID9925681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:32846938..32850876hg38UCSC Ensembl
Outerchr11:32846781..32851029hg38UCSC Ensembl
Innerchr11:32868484..32872422hg19UCSC Ensembl
Outerchr11:32868327..32872575hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384249
hg194249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5633045, essv5466912, essv5474333, essv6568516
SamplesNA20537, NA19371, NA19434, NA19316
Known GenesPRRG4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659576
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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