A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14189736



Internal ID1514904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65249890..65257658hg38UCSC Ensembl
Innerchr11:65249890..65257658hg38UCSC Ensembl
Outerchr11:65249832..65257757hg38UCSC Ensembl
chr11:65017361..65025129hg19UCSC Ensembl
Innerchr11:65017361..65025129hg19UCSC Ensembl
Outerchr11:65017303..65025228hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387769
hg197769
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626670
Supporting Variants
SamplesHG01392
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14189736
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