A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4606n100



Internal ID20156222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18655..164435hg38UCSC Ensembl
chr3:60333..206118hg19UCSC Ensembl
chr3:35333..181118hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38145781
hg19145786
hg18145786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013078, nsv998095, nsv997648, nsv1010197, nsv1011475, nsv1008998, nsv1001399, nsv1002045, nsv1007289, nsv1009462
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)dgv4606n100
Frequency
Sample Size29084
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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