A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546168



Internal ID15986891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47416306..47416444hg38UCSC Ensembl
Innerchr1:47881978..47882116hg19UCSC Ensembl
Innerchr1:47654565..47654703hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38139
hg19139
hg18139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712904
Samples
Known GenesFOXE3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546168
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