A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151252



Internal ID15855391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16551808..16813361hg38UCSC Ensembl
Innerchr22:17032698..17294251hg19UCSC Ensembl
Innerchr22:15412698..15674251hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38261554
hg19261554
hg18261554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588074
Supporting Variants
Samples1780862579_A
Known GenesANKRD62P1-PARP4P3, CCT8L2, TPTEP1, XKR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151252
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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