A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6267803



Internal ID9741006
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 StatusS
Merged Variantsesv2664926
Supporting Variants
SamplesNA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6267803
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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