A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038920



Internal ID18781451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33120512..33461427hg38UCSC Ensembl
Innerchr11:33142058..33482973hg19UCSC Ensembl
Innerchr11:33098634..33439549hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38340916
hg19340916
hg18340916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1093n100
Supporting Variantsnssv3506874
Samples
Known GenesCSTF3, CSTF3-AS1, HIPK3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038920
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