A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047794



Internal ID18790325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5982198..6094875hg38UCSC Ensembl
Innerchr11:6003428..6116105hg19UCSC Ensembl
Innerchr11:5960004..6072681hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38112678
hg19112678
hg18112678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1054n100
Supporting Variantsnssv3708504
Samples
Known GenesOR52L1, OR56A1, OR56A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047794
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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