A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588874



Internal ID16376283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27154802..27179580hg38UCSC Ensembl
Innerchr22:27550764..27575542hg19UCSC Ensembl
Innerchr22:25880764..25905542hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3824779
hg1924779
hg1824779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8082n54
Supporting Variantsnssv954552
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588874
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