A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524400



Internal ID15105007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5307131..5395392hg38UCSC Ensembl
Innerchr11:5328361..5416622hg19UCSC Ensembl
Innerchr11:5284937..5373198hg18UCSC Ensembl
Innerchr11:5284937..5373198hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3888262
hg1988262
hg1888262
hg1788262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700318
Samples
Known GenesOR51B2, OR51B5, OR51B6, OR51M1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524400
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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