A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589028



Internal ID16376437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38976422..38988748hg38UCSC Ensembl
Innerchr22:39372427..39384753hg19UCSC Ensembl
Innerchr22:37702373..37714699hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3812327
hg1912327
hg1812327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8107n54
Supporting Variantsnssv957059
Samples
Known GenesAPOBEC3A_B, APOBEC3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589028
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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