A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14025035



Internal ID5431504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9563051..9564419hg38UCSC Ensembl
Innerchr11:9563051..9564419hg38UCSC Ensembl
Outerchr11:9562850..9564756hg38UCSC Ensembl
chr11:9584598..9585966hg19UCSC Ensembl
Innerchr11:9584598..9585966hg19UCSC Ensembl
Outerchr11:9584397..9586303hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625337
Supporting Variants
SamplesNA18956
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14025035
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