A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14088477



Internal ID2321632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33848531..33851312hg38UCSC Ensembl
Innerchr11:33848533..33851310hg38UCSC Ensembl
Outerchr11:33848529..33851314hg38UCSC Ensembl
chr11:33870077..33872858hg19UCSC Ensembl
Innerchr11:33870079..33872856hg19UCSC Ensembl
Outerchr11:33870075..33872860hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382782
hg192782
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625898
Supporting Variants
SamplesHG02067
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14088477
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