A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589029



Internal ID16376438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38976422..38992223hg38UCSC Ensembl
Innerchr22:39372427..39388228hg19UCSC Ensembl
Innerchr22:37702373..37718174hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3815802
hg1915802
hg1815802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8107n54
Supporting Variantsnssv957060
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)nsv589029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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