A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5441n100



Internal ID22791528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152321467..152413464hg38UCSC Ensembl
chr4:153242619..153334616hg19UCSC Ensembl
chr4:153462069..153554066hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3891998
hg1991998
hg1891998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017089, nsv1019479, nsv1023383
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)dgv5441n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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