A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040728



Internal ID18783259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55587591..55674830hg38UCSC Ensembl
Innerchr11:55355067..55442306hg19UCSC Ensembl
Innerchr11:55111643..55198882hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3887240
hg1987240
hg1887240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1176n100
Supporting Variantsnssv3506108
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040728
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer