A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1075n100



Internal ID22787162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23774916..23862068hg38UCSC Ensembl
chr11:23796462..23883614hg19UCSC Ensembl
chr11:23753038..23840190hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3887153
hg1987153
hg1887153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054249, nsv1054145, nsv1053104
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1075n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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