A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589084



Internal ID16029807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:42776261..42807131hg38UCSC Ensembl
Innerchr22:43172267..43203137hg19UCSC Ensembl
Innerchr22:41502211..41533081hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3830871
hg1930871
hg1830871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957172
Samples
Known GenesARFGAP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589084
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