A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3051n100



Internal ID20154667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82138730..83654472hg38UCSC Ensembl
chr16:82172335..83688077hg19UCSC Ensembl
chr16:80729836..82245578hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381515743
hg191515743
hg181515743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065965, nsv1060851
Samples
Known GenesCDH13, MIR3182, MIR8058, MPHOSPH6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3051n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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