A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659539



Internal ID9925644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85718809..85761155hg38UCSC Ensembl
Outerchr11:85718772..85761205hg38UCSC Ensembl
Innerchr11:85429852..85472198hg19UCSC Ensembl
Outerchr11:85429815..85472248hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3842434
hg1942434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5739256
SamplesNA12761
Known GenesSYTL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659539
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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