A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759782



Internal ID18711377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89298100..89438209hg38UCSC Ensembl
Innerchr9:91913015..92053124hg19UCSC Ensembl
Innerchr9:91102835..91242944hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38140110
hg19140110
hg18140110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041327
Supporting Variants
Samples
Known GenesCKS2, MIR3153, SECISBP2, SEMA4D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3759782
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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