A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14241881



Internal ID2418691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94933728..94938925hg38UCSC Ensembl
Innerchr11:94933743..94938911hg38UCSC Ensembl
Outerchr11:94933714..94938940hg38UCSC Ensembl
chr11:94666893..94672090hg19UCSC Ensembl
Innerchr11:94666908..94672076hg19UCSC Ensembl
Outerchr11:94666879..94672105hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385198
hg195198
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627335
Supporting Variants
SamplesHG02139
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14241881
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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