A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8920n54



Internal ID22776815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2531805..2548745hg38UCSC Ensembl
chr4:2533532..2550472hg19UCSC Ensembl
chr4:2503330..2520270hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3816941
hg1916941
hg1816941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593422, nsv593421, nsv593433
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8920n54
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