A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056597



Internal ID18799128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38950674..38993688hg38UCSC Ensembl
Innerchr22:39346679..39389693hg19UCSC Ensembl
Innerchr22:37676625..37719639hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3843015
hg1943015
hg1843015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734211
Samples
Known GenesAPOBEC3A, APOBEC3A_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)nsv1056597
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer