A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666133



Internal ID9585552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34891880..34899608hg38UCSC Ensembl
chr11:34913427..34921155hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387729
hg197729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5678414
SamplesNA11992
Known GenesAPIP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666133
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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