A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789744



Internal ID19162262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90290567..90393775hg38UCSC Ensembl
Innerchr3:90339717..90442925hg19UCSC Ensembl
Innerchr3:90422407..90525615hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38103209
hg19103209
hg18103209
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893740
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789744
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