A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059522



Internal ID18802053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33310215..33332496hg38UCSC Ensembl
Innerchr22:33706201..33728482hg19UCSC Ensembl
Innerchr22:32036201..32058482hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3822282
hg1922282
hg1822282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600827
Samples
Known GenesLARGE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059522
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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