A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063410



Internal ID18805941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36225663..36317486hg38UCSC Ensembl
Innerchr22:36621709..36713531hg19UCSC Ensembl
Innerchr22:34951655..35043477hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3891824
hg1991823
hg1891823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4564n100
Supporting Variantsnssv3600864, nssv3600860, nssv3600859, nssv3600858, nssv3600855, nssv3600861, nssv3600862, nssv3600863, nssv3600857, nssv3600856
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)nsv1063410
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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