A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14233973



Internal ID6905443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91749023..91756430hg38UCSC Ensembl
Innerchr11:91749033..91756421hg38UCSC Ensembl
Outerchr11:91749014..91756440hg38UCSC Ensembl
chr11:91482189..91489596hg19UCSC Ensembl
Innerchr11:91482199..91489587hg19UCSC Ensembl
Outerchr11:91482180..91489606hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg387408
hg197408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627259
Supporting Variants
SamplesNA21111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14233973
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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