A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589026



Internal ID16376435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38969771..38992041hg38UCSC Ensembl
Innerchr22:39365776..39388046hg19UCSC Ensembl
Innerchr22:37695722..37717992hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3822271
hg1922271
hg1822271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8106n54
Supporting Variantsnssv957051, nssv957047, nssv957046, nssv957054, nssv957055, nssv957045, nssv957048, nssv957043, nssv957050, nssv957053, nssv957044, nssv957052, nssv957049
Samples
Known GenesAPOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589026
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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