A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663781



Internal ID9929886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117217227..117223275hg38UCSC Ensembl
Outerchr10:117217193..117223310hg38UCSC Ensembl
Innerchr10:118976738..118982786hg19UCSC Ensembl
Outerchr10:118976704..118982821hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg386118
hg196118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6078771
SamplesNA19313
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663781
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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