A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1014n100



Internal ID20152630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1264737..1397647hg38UCSC Ensembl
chr11:1285967..1418877hg19UCSC Ensembl
chr11:1242543..1375453hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38132911
hg19132911
hg18132911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036407, nsv1035740
Samples
Known GenesBRSK2, TOLLIP, TOLLIP-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1014n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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