A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5889n100



Internal ID22791976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:280387..365708hg38UCSC Ensembl
chr6:280387..365708hg19UCSC Ensembl
chr6:225387..310708hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3885322
hg1985322
hg1885322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019439, nsv1017714, nsv1015946, nsv1034062
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5889n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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