A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1274n100



Internal ID20152890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107597955..108083284hg38UCSC Ensembl
chr11:107468681..107954011hg19UCSC Ensembl
chr11:106973891..107459221hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38485330
hg19485331
hg18485331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049524, nsv1039425
Samples
Known GenesCUL5, ELMOD1, RAB39A, SLC35F2, SLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1274n100
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