A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788110



Internal ID19160514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:45701407..46378855hg38UCSC Ensembl
Innerchr5:45701509..46378957hg19UCSC Ensembl
Innerchr5:45737266..46414714hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38677449
hg19677449
hg18677449
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894185
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788110
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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