A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546165



Internal ID15986888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:46800918..46807113hg38UCSC Ensembl
Innerchr1:47266590..47272785hg19UCSC Ensembl
Innerchr1:47039177..47045372hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg386196
hg196196
hg186196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712902
Samples
Known GenesCYP4B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546165
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