A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5440n100



Internal ID20157056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152321467..152392321hg38UCSC Ensembl
chr4:153242619..153313473hg19UCSC Ensembl
chr4:153462069..153532923hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3870855
hg1970855
hg1870855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024703, nsv1024767, nsv1028139, nsv1029277, nsv1024010, nsv1030237, nsv1032762, nsv1016911, nsv1025167, nsv1031547, nsv1023364
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)dgv5440n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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