A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8489n54



Internal ID22776384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104359848..104560158hg38UCSC Ensembl
chr3:104078692..104279002hg19UCSC Ensembl
chr3:105561382..105761692hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38200311
hg19200311
hg18200311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591214, nsv591213
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8489n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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