A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788996



Internal ID19166781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:269147..336332hg38UCSC Ensembl
Innerchr11:269147..336332hg19UCSC Ensembl
Innerchr11:259147..326332hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3867186
hg1967186
hg1867186
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891905
Supporting Variants
Samples
Known GenesATHL1, IFITM1, IFITM2, IFITM3, IFITM5, NLRP6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788996
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