A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14088616



Internal ID5410339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34199171..34204543hg38UCSC Ensembl
Innerchr11:34199171..34204543hg38UCSC Ensembl
Outerchr11:34198964..34204818hg38UCSC Ensembl
chr11:34220718..34226090hg19UCSC Ensembl
Innerchr11:34220718..34226090hg19UCSC Ensembl
Outerchr11:34220511..34226365hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385373
hg195373
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625908
Supporting Variants
SamplesNA18947
Known GenesABTB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14088616
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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