A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14049821



Internal ID5876254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22093542..22101631hg38UCSC Ensembl
Innerchr11:22094042..22101131hg38UCSC Ensembl
Outerchr11:22092542..22102631hg38UCSC Ensembl
chr11:22115088..22123177hg19UCSC Ensembl
Innerchr11:22115588..22122677hg19UCSC Ensembl
Outerchr11:22114088..22124177hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg388090
hg198090
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625610
Supporting Variants
SamplesNA19257
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14049821
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