A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15091135



Internal ID4723060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86419380..86457635hg38UCSC Ensembl
chr14:86885724..86923979hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3838256
hg1938256
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635231
Supporting Variants
SamplesNA06984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15091135
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