A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064449



Internal ID18806980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36225663..36309372hg38UCSC Ensembl
Innerchr22:36621709..36705417hg19UCSC Ensembl
Innerchr22:34951655..35035363hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3883710
hg1983709
hg1883709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4564n100
Supporting Variantsnssv3600852
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)nsv1064449
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