A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5765324



Internal ID8742727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3882367..3885322hg38UCSC Ensembl
Outerchr11:3882210..3885475hg38UCSC Ensembl
Innerchr11:3903597..3906552hg19UCSC Ensembl
Outerchr11:3903440..3906705hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383266
hg193266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672740
Supporting Variants
SamplesHG00525
Known GenesSTIM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5765324
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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