A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549181



Internal ID15989904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:214606866..214609149hg38UCSC Ensembl
Innerchr1:214780209..214782492hg19UCSC Ensembl
Innerchr1:212846832..212849115hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382284
hg192284
hg182284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv736936
Samples
Known GenesCENPF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549181
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