A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712395



Internal ID18663990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55473527..55614334hg38UCSC Ensembl
Innerchr11:55241003..55381810hg19UCSC Ensembl
Innerchr11:54997579..55138386hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38140808
hg19140808
hg18140808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046475
Supporting Variants
Samples
Known GenesOR4C11, OR4C15, OR4C16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712395
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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