A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14278412



Internal ID5967623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108468960..108470813hg38UCSC Ensembl
Innerchr11:108468985..108470789hg38UCSC Ensembl
Outerchr11:108468936..108470838hg38UCSC Ensembl
chr11:108339687..108341540hg19UCSC Ensembl
Innerchr11:108339712..108341516hg19UCSC Ensembl
Outerchr11:108339663..108341565hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381854
hg191854
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627678
Supporting Variants
SamplesNA19379
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14278412
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer