A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv773968



Internal ID15721238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49824008..50162830hg38UCSC Ensembl
Innerchr11:49845560..50122001hg19UCSC Ensembl
Innerchr11:49802136..50078577hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38338823
hg19276442
hg18276442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554393
Supporting Variants
Samples
Known GenesOR4C12, OR4C13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv773968
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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