A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1959n100



Internal ID22788046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94178251..94254190hg38UCSC Ensembl
chr14:94644588..94720527hg19UCSC Ensembl
chr14:93714341..93790280hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3875940
hg1975940
hg1875940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037842, nsv1046206
Samples
Known GenesPPP4R4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1959n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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