A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520914



Internal ID18819195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55654851..55835981hg38UCSC Ensembl
Innerchr11:55422327..55603457hg19UCSC Ensembl
Innerchr11:55178903..55360033hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38181131
hg19181131
hg18181131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053172
Supporting Variants
Samples
Known GenesOR4C6, OR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520914
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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