A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553161



Internal ID16340570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4382962..4568550hg38UCSC Ensembl
Innerchr11:4404192..4589780hg19UCSC Ensembl
Innerchr11:4360768..4546356hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38185589
hg19185589
hg18185589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1583n54
Supporting Variantsnssv764650
Samples
Known GenesOR52K1, OR52K2, OR52M1, TRIM21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553161
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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