A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4684n100



Internal ID22790771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11892508..11915124hg38UCSC Ensembl
chr3:11933982..11956598hg19UCSC Ensembl
chr3:11908982..11931598hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3822617
hg1922617
hg1822617
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000618, nsv1008224, nsv998630, nsv1006222, nsv1000405
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4684n100
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