A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6259211



Internal ID9236614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124332481..124404353hg38UCSC Ensembl
chr11:124202377..124274249hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3871873
hg1971873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658517
Supporting Variants
SamplesNA12775
Known GenesOR8B2, OR8B3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6259211
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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