A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4734n100



Internal ID20156350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46751875..46818330hg38UCSC Ensembl
chr3:46793365..46859820hg19UCSC Ensembl
chr3:46768369..46834824hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3866456
hg1966456
hg1866456
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001783, nsv1014321
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)dgv4734n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss66
Observed Complex0
Frequencyn/a


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