A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4605n100



Internal ID20156221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18655..115870hg38UCSC Ensembl
chr3:60333..157553hg19UCSC Ensembl
chr3:35333..132553hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3897216
hg1997221
hg1897221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003910, nsv1008987, nsv1002126, nsv1002577, nsv1004219, nsv1008169, nsv1005233, nsv1003412, nsv997453, nsv997387, nsv1000721, nsv1012315, nsv1014700, nsv1001171, nsv1010822, nsv998594
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)dgv4605n100
Frequency
Sample Size29084
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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