A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063231



Internal ID18805762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36225663..36314496hg38UCSC Ensembl
Innerchr22:36621709..36710541hg19UCSC Ensembl
Innerchr22:34951655..35040487hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3888834
hg1988833
hg1888833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4564n100
Supporting Variantsnssv3600854
Samples
Known GenesAPOL1, APOL2, MIR6819, MYH9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063231
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