A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510817



Internal ID18462412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55584048..55662485hg38UCSC Ensembl
Innerchr11:55351524..55429961hg19UCSC Ensembl
Innerchr11:55108100..55186537hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3878438
hg1978438
hg1878438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053726
Supporting Variants
Samples
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510817
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer