A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661233



Internal ID9580652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12886179..12887380hg38UCSC Ensembl
chr11:12907726..12908927hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv193e199
Supporting Variantsessv5565674
SamplesNA19082
Known GenesTEAD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661233
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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