A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4819n100



Internal ID20156435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98565439..98662629hg38UCSC Ensembl
chr3:98284283..98381473hg19UCSC Ensembl
chr3:99766973..99864163hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3897191
hg1997191
hg1897191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000357, nsv997484
Samples
Known GenesCPOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4819n100
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