A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5438n100



Internal ID22791525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151870381..151957945hg38UCSC Ensembl
chr4:152791533..152879097hg19UCSC Ensembl
chr4:153010983..153098547hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3887565
hg1987565
hg1887565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028836, nsv1030328
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5438n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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