A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678898



Internal ID9945003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43457847..43463757hg38UCSC Ensembl
Outerchr11:43457690..43463910hg38UCSC Ensembl
Innerchr11:43479397..43485307hg19UCSC Ensembl
Outerchr11:43479240..43485460hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386221
hg196221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5544802
SamplesNA19471
Known GenesTTC17
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678898
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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