A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661859



Internal ID4706193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:111531862..111536818hg19UCSC Ensembl
Outerchr6:111531825..111536868hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv5551919
SamplesNA18553
Known GenesSLC16A10
Method
Analysis
Platform
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661859
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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