A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4571n100



Internal ID22790658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38967602..39003295hg38UCSC Ensembl
chr22:39363607..39399300hg19UCSC Ensembl
chr22:37693553..37729246hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3835694
hg1935694
hg1835694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064318, nsv1059714, nsv1061959, nsv1059547, nsv1062093, nsv1060743
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)dgv4571n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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