A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14004625



Internal ID2781904
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625246
Supporting Variants
SamplesHG02455
Known GenesTRIM5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14004625
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