A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv767056



Internal ID16061012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8937473..8943144hg38UCSC Ensembl
Innerchr11:8959020..8964691hg19UCSC Ensembl
Innerchr11:8915596..8921267hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385672
hg195672
hg185672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553452
Supporting Variants
Samples
Known GenesASCL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv767056
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