A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035355



Internal ID19124574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4784692..4886442hg38UCSC Ensembl
Innerchr11:4805922..4907672hg19UCSC Ensembl
Innerchr11:4762498..4864248hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38101751
hg19101751
hg18101751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1026n100
Supporting Variantsnssv3510480, nssv3706408
Samples
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035355
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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