A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1466n100



Internal ID22787553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:37463949..37714239hg38UCSC Ensembl
chr12:37857751..38108041hg19UCSC Ensembl
chr12:36144018..36394308hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38250291
hg19250291
hg18250291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054862, nsv1038938
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)dgv1466n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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