A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503472



Internal ID18455067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:47773069..48644472hg38UCSC Ensembl
Innerchr11:47794621..48666024hg19UCSC Ensembl
Innerchr11:47751197..48622600hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38871404
hg19871404
hg18871404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036992
Supporting Variants
Samples
Known GenesNUP160, OR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3503472
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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