A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4892n54



Internal ID20138316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6699870..7091209hg38UCSC Ensembl
chr16:6749871..7141210hg19UCSC Ensembl
chr16:6689872..7081211hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38391340
hg19391340
hg18391340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571351, nsv571354, nsv571349, nsv571350, nsv571352
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4892n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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