A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664926



Internal ID9931031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66536622..66537679hg38UCSC Ensembl
chr11:66304093..66305150hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6546664, essv5737834, essv5747787, essv6205152, essv5437947, essv5846920, essv6267803
SamplesHG00189, NA12761, HG00275, HG00276, HG00146, HG00377, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664926
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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