A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671948



Internal ID9591367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94349534..94645424hg38UCSC Ensembl
chr11:94082700..94378590hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38295891
hg19295891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6109525
SamplesHG00578
Known GenesANKRD49, FUT4, GPR83, LOC643037, MRE11A, PIWIL4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671948
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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