A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789209



Internal ID19168175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107785223..107800900hg38UCSC Ensembl
Innerchr11:107655949..107671626hg19UCSC Ensembl
Innerchr11:107161159..107176836hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3815678
hg1915678
hg1815678
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892099
Supporting Variants
Samples
Known GenesSLC35F2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789209
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