A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546169



Internal ID15986892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47416306..47417347hg38UCSC Ensembl
Innerchr1:47881978..47883019hg19UCSC Ensembl
Innerchr1:47654565..47655606hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg381042
hg191042
hg181042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712905
Samples
Known GenesFOXE3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546169
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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