A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525475



Internal ID15452768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21840786..21851322hg38UCSC Ensembl
Innerchr22:22195075..22205611hg19UCSC Ensembl
Innerchr22:20525075..20535611hg18UCSC Ensembl
Innerchr22:20519629..20530165hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3810537
hg1910537
hg1810537
hg1710537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv256n21
Supporting Variantsnssv701603
Samples
Known GenesMAPK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525475
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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