A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14234130



Internal ID767192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92291521..92294805hg38UCSC Ensembl
Innerchr11:92291522..92294805hg38UCSC Ensembl
Outerchr11:92291521..92294806hg38UCSC Ensembl
chr11:92024687..92027971hg19UCSC Ensembl
Innerchr11:92024688..92027971hg19UCSC Ensembl
Outerchr11:92024687..92027972hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383285
hg193285
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627272
Supporting Variants
SamplesHG00362
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14234130
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