A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv192e199



Internal ID22757965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9615605..9617615hg38UCSC Ensembl
chr11:9637152..9639162hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382011
hg192011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2667778, esv2677548
SamplesNA18544
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv192e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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