A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790839



Internal ID19164398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148766..427832hg38UCSC Ensembl
Innerchr4:142550..421621hg19UCSC Ensembl
Innerchr4:132550..411621hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38279067
hg19279072
hg18279072
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893862
Supporting Variants
Samples
Known GenesABCA11P, ZNF141, ZNF718, ZNF732, ZNF876P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=49
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790839
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