A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3665n100



Internal ID22789752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54639933..54664828hg38UCSC Ensembl
chr19:55151384..55176279hg19UCSC Ensembl
chr19:59843196..59868091hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3824896
hg1924896
hg1824896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064009, nsv1067560
Samples
Known GenesLILRB4, MIR8061
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3665n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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