A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661859



Internal ID2894946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:111210659..111215615hg38UCSC Ensembl
Outerchr6:111210622..111215665hg38UCSC Ensembl
Innerchr6:111531862..111536818hg19UCSC Ensembl
Outerchr6:111531825..111536868hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385044
hg195044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5551919
SamplesNA18553
Known GenesSLC16A10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
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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