A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061802



Internal ID18804333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36236979..36315794hg38UCSC Ensembl
Innerchr22:36633025..36711839hg19UCSC Ensembl
Innerchr22:34962971..35041785hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3878816
hg1978815
hg1878815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4564n100
Supporting Variantsnssv3600868
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)nsv1061802
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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