A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061176



Internal ID18803707
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590745, nssv3590746, nssv3590749, nssv3590748, nssv3590747
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)nsv1061176
Frequency
Sample Size29084
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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