A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5412n100



Internal ID22791499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143773621..143837051hg38UCSC Ensembl
chr4:144694774..144758204hg19UCSC Ensembl
chr4:144914224..144977654hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3863431
hg1963431
hg1863431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033043, nsv1033830
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)dgv5412n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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