A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792733



Internal ID19182965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91494378..91829243hg38UCSC Ensembl
Innerchr4:92415529..92750394hg19UCSC Ensembl
Innerchr4:92634552..92969417hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38334866
hg19334866
hg18334866
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893986
Supporting Variants
Samples
Known GenesCCSER1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=55
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792733
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