A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666997



Internal ID9586416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61881721..61885725hg38UCSC Ensembl
Outerchr11:61881684..61885775hg38UCSC Ensembl
Innerchr11:61649193..61653197hg19UCSC Ensembl
Outerchr11:61649156..61653247hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg384092
hg194092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv217e199
Supporting Variantsessv5762232
SamplesNA19471
Known GenesFADS3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666997
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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