A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13998746



Internal ID4186064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4368636..4429909hg38UCSC Ensembl
chr11:4389866..4451139hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3861274
hg1961274
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625183
Supporting Variants
SamplesHG03779
Known GenesTRIM21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13998746
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer