A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656806



Internal ID9576225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87042798..87045470hg38UCSC Ensembl
Outerchr11:87042641..87045623hg38UCSC Ensembl
Innerchr11:86753840..86756512hg19UCSC Ensembl
Outerchr11:86753683..86756665hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382983
hg192983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6294702
SamplesNA19213
Known GenesTMEM135
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656806
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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