A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6487539



Internal ID8873605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33068293..33068574hg38UCSC Ensembl
chr11:33089839..33090120hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658399
Supporting Variants
SamplesHG00326
Known GenesTCP11L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6487539
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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