A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518089



Internal ID18816370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9231310..9517330hg38UCSC Ensembl
Innerchr11:9252857..9538877hg19UCSC Ensembl
Innerchr11:9209433..9495453hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38286021
hg19286021
hg18286021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055078
Supporting Variants
Samples
Known GenesDENND5A, IPO7, LOC644656, SNORA23, TMEM41B, ZNF143
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518089
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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