A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553306



Internal ID16340715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5754500..5784285hg38UCSC Ensembl
Innerchr11:5775730..5805515hg19UCSC Ensembl
Innerchr11:5732306..5762091hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3829786
hg1929786
hg1829786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1616n54
Supporting Variantsnssv765900
Samples
Known GenesOR52N4, OR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553306
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