A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5789002



Internal ID8766405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16201613..16201932hg38UCSC Ensembl
chr11:16223159..16223478hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666456
Supporting Variants
SamplesNA18562
Known GenesSOX6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5789002
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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