A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5934596



Internal ID8911999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122917875..122918925hg38UCSC Ensembl
chr11:122788583..122789633hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381051
hg191051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661962
Supporting Variants
SamplesNA19130
Known GenesC11orf63
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5934596
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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