A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041634



Internal ID19130853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6733987..6788217hg38UCSC Ensembl
Innerchr11:6755218..6809448hg19UCSC Ensembl
Innerchr11:6711794..6766024hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3854231
hg1954231
hg1854231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1055n100
Supporting Variantsnssv3513280
Samples
Known GenesOR2AG1, OR2AG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041634
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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