A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791596



Internal ID19171424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:110391186..111054206hg38UCSC Ensembl
Innerchr3:110110033..110773053hg19UCSC Ensembl
Innerchr3:111592723..112255743hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38663021
hg19663021
hg18663021
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893762
Supporting Variants
Samples
Known GenesPVRL3-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=81
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791596
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