A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590749



Internal ID18889030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967602..38999490hg38UCSC Ensembl
Innerchr22:39363607..39395495hg19UCSC Ensembl
Innerchr22:37693553..37725441hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3831889
hg1931889
hg1831889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061176
Supporting Variants
Samples
Known GenesAPOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3590749
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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