A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055716



Internal ID18798247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967602..39010177hg38UCSC Ensembl
Innerchr22:39363607..39406182hg19UCSC Ensembl
Innerchr22:37693553..37736128hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3842576
hg1942576
hg1842576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590752
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)nsv1055716
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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