A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5442n100



Internal ID22791529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152331622..152388386hg38UCSC Ensembl
chr4:153252774..153309538hg19UCSC Ensembl
chr4:153472224..153528988hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3856765
hg1956765
hg1856765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022791, nsv1017583, nsv1031444, nsv1026334, nsv1031884
Samples
Known GenesDEAR, FBXW7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5442n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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