A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3507194



Internal ID18805475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89558524..89878164hg38UCSC Ensembl
Innerchr11:89291692..89611332hg19UCSC Ensembl
Innerchr11:88931340..89250980hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38319641
hg19319641
hg18319641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043643
Supporting Variants
Samples
Known GenesFOLH1B, MIR5692A1, NOX4, TRIM49, TRIM53AP, TRIM64B, TRIM77
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3507194
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