A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046298



Internal ID19135517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5761870..5788219hg38UCSC Ensembl
Innerchr11:5783100..5809449hg19UCSC Ensembl
Innerchr11:5739676..5766025hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826350
hg1926350
hg1826350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1044n100
Supporting Variantsnssv3507246, nssv3521488, nssv3517279
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046298
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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