A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1551n100



Internal ID22787638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105673271..105852804hg38UCSC Ensembl
chr12:106067049..106246582hg19UCSC Ensembl
chr12:104591179..104770712hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38179534
hg19179534
hg18179534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040261, nsv1047810
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)dgv1551n100
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