A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1216n100



Internal ID20152832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67715176..67981775hg38UCSC Ensembl
chr11:67482647..67749246hg19UCSC Ensembl
chr11:67239223..67505822hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38266600
hg19266600
hg18266600
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036727, nsv1049462, nsv1049386, nsv1046695
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1216n100
Frequency
Sample Size29084
Observed Gain21
Observed Loss5
Observed Complex0
Frequencyn/a


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