A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9419n54



Internal ID22777314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184825378..184826384hg38UCSC Ensembl
chr4:185746532..185747538hg19UCSC Ensembl
chr4:185983526..185984532hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381007
hg191007
hg181007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596357, nsv596353, nsv596359, nsv596360, nsv596356
Samples
Known GenesACSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9419n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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