A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546188



Internal ID15986911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47417089..47417347hg38UCSC Ensembl
Innerchr1:47882761..47883019hg19UCSC Ensembl
Innerchr1:47655348..47655606hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38259
hg19259
hg18259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712957
Samples
Known GenesFOXE3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546188
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