A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14204906



Internal ID5105309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69218226..69232991hg38UCSC Ensembl
Innerchr11:69218252..69232965hg38UCSC Ensembl
Outerchr11:69218200..69233017hg38UCSC Ensembl
chr11:68985693..69000458hg19UCSC Ensembl
Innerchr11:68985719..69000432hg19UCSC Ensembl
Outerchr11:68985667..69000484hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3814766
hg1914766
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626745
Supporting Variants
SamplesNA18557
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14204906
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