A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8106n54



Internal ID20141530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38969771..38992223hg38UCSC Ensembl
chr22:39365776..39388228hg19UCSC Ensembl
chr22:37695722..37718174hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3822453
hg1922453
hg1822453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589024, nsv589022, nsv589026, nsv589027, nsv589023, nsv589025
Samples
Known GenesAPOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8106n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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