A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590777



Internal ID18889058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967667..38979290hg38UCSC Ensembl
Innerchr22:39363672..39375295hg19UCSC Ensembl
Innerchr22:37693618..37705241hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3811624
hg1911624
hg1811624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055560
Supporting Variants
Samples
Known GenesAPOBEC3A_B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3590777
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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