A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3316n100



Internal ID20154932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4454150..4494321hg38UCSC Ensembl
chr18:4454150..4494321hg19UCSC Ensembl
chr18:4444150..4484321hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3840172
hg1940172
hg1840172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062733, nsv1060866, nsv1060195, nsv1060284
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3316n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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