A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787836



Internal ID19164642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103978774..104885172hg38UCSC Ensembl
Innerchr5:103314475..104220873hg19UCSC Ensembl
Innerchr5:103342374..104248772hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg38906399
hg19906399
hg18906399
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890691
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=138
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787836
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