A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522846



Internal ID15103453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55555063..55628565hg38UCSC Ensembl
Innerchr11:55322539..55396041hg19UCSC Ensembl
Innerchr11:55079115..55152617hg18UCSC Ensembl
Innerchr11:55079115..55152617hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3873503
hg1973503
hg1873503
hg1773503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698499
Samples
Known GenesOR4C11, OR4C15, OR4C16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522846
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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