A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957063



Internal ID15904333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39077624..39086804hg38UCSC Ensembl
Innerchr22:39473629..39482809hg19UCSC Ensembl
Innerchr22:37803575..37812755hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg389181
hg199181
hg189181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589032
Supporting Variants
Samples
Known GenesAPOBEC3G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957063
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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