A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553407



Internal ID15994130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7664234..7665353hg38UCSC Ensembl
Innerchr11:7685465..7686584hg19UCSC Ensembl
Innerchr11:7642041..7643160hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381120
hg191120
hg181120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv766939
Samples
Known GenesCYB5R2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553407
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