A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625246



Internal ID7012081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5684567..5687164hg38UCSC Ensembl
Innerchr11:5684567..5687164hg38UCSC Ensembl
Outerchr11:5684431..5687304hg38UCSC Ensembl
chr11:5705797..5708394hg19UCSC Ensembl
Innerchr11:5705797..5708394hg19UCSC Ensembl
Outerchr11:5705661..5708534hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382598
hg192598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14004625
SamplesHG02455
Known GenesTRIM5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625246
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