A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589025



Internal ID16376434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38969771..38990107hg38UCSC Ensembl
Innerchr22:39365776..39386112hg19UCSC Ensembl
Innerchr22:37695722..37716058hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3820337
hg1920337
hg1820337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8106n54
Supporting Variantsnssv957042, nssv957041, nssv957039, nssv957040
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)nsv589025
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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