A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673543



Internal ID9939648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40014850..40020308hg38UCSC Ensembl
Innerchr11:40036400..40041858hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385459
hg195459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5768574, essv5469633
SamplesNA18547, NA18573
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673543
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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