A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5960n100



Internal ID20157576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49322472..49684411hg38UCSC Ensembl
chr6:49290141..49652124hg19UCSC Ensembl
chr6:49398100..49760083hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38361940
hg19361984
hg18361984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024959, nsv1021136
Samples
Known GenesC6orf141, CENPQ, GLYATL3, MUT, RHAG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5960n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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