A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589225



Internal ID16376634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:50624510..50663510hg38UCSC Ensembl
Innerchr22:51062938..51101938hg19UCSC Ensembl
Innerchr22:49409804..49448804hg18UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3839001
hg1939001
hg1839001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957543
Samples
Known GenesARSA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589225
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