A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589031



Internal ID16029754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38988347..38992041hg38UCSC Ensembl
Innerchr22:39384352..39388046hg19UCSC Ensembl
Innerchr22:37714298..37717992hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383695
hg193695
hg183695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957062
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)nsv589031
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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