A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852395



Internal ID15799665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6812010..6913769hg38UCSC Ensembl
Innerchr16:6862011..6963770hg19UCSC Ensembl
Innerchr16:6802012..6903771hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38101760
hg19101760
hg18101760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571368
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852395
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