A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066354



Internal ID18808885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39070438..39130755hg38UCSC Ensembl
Innerchr22:39466443..39526760hg19UCSC Ensembl
Innerchr22:37796389..37856706hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3860318
hg1960318
hg1860318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590785
Samples
Known GenesAPOBEC3G, APOBEC3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066354
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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