A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787774



Internal ID19161714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168175986..168229728hg38UCSC Ensembl
Innerchr3:167893774..167947516hg19UCSC Ensembl
Innerchr3:169376468..169430210hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3853743
hg1953743
hg1853743
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893810
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787774
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