A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8636n54



Internal ID22776531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149227668..149251541hg38UCSC Ensembl
chr3:148945455..148969328hg19UCSC Ensembl
chr3:150428145..150452018hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3823874
hg1923874
hg1823874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591974, nsv591972, nsv591973
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8636n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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