A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045734



Internal ID18788265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48067763..48871655hg38UCSC Ensembl
Innerchr11:48089315..48893207hg19UCSC Ensembl
Innerchr11:48045891..48849783hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38803893
hg19803893
hg18803893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1112n100
Supporting Variantsnssv3710121
Samples
Known GenesOR4A47, 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)nsv1045734
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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