A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4569n100



Internal ID20156185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38954022..38979290hg38UCSC Ensembl
chr22:39350027..39375295hg19UCSC Ensembl
chr22:37679973..37705241hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3825269
hg1925269
hg1825269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061241, nsv1064826, nsv1061793, nsv1061040
Samples
Known GenesAPOBEC3A, APOBEC3A_B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4569n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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