A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712399



Internal ID18663994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55593873..55672502hg38UCSC Ensembl
Innerchr11:55361349..55439978hg19UCSC Ensembl
Innerchr11:55117925..55196554hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3878630
hg1978630
hg1878630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045845
Supporting Variants
Samples
Known GenesOR4C11, OR4C6, 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)nssv3712399
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