A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066496



Internal ID18809027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:50226183..50292445hg38UCSC Ensembl
Innerchr22:50664612..50730874hg19UCSC Ensembl
Innerchr22:49006739..49073001hg18UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3866263
hg1966263
hg1866263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737504
Samples
Known GenesHDAC10, MAPK11, MAPK12, PLXNB2, TUBGCP6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066496
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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