A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059368



Internal ID19148587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:32853134..32872795hg38UCSC Ensembl
Innerchr22:33249121..33268782hg19UCSC Ensembl
Innerchr22:31579121..31598782hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3819662
hg1919662
hg1819662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600824
Samples
Known GenesSYN3, TIMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059368
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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