A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059314



Internal ID18801845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:31497627..31540102hg38UCSC Ensembl
Innerchr22:31893613..31936088hg19UCSC Ensembl
Innerchr22:30223613..30266088hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3842476
hg1942476
hg1842476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600810, nssv3600809
Samples
Known GenesSFI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059314
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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