A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1855n100



Internal ID22787942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26365363..26392849hg38UCSC Ensembl
chr14:26834569..26862055hg19UCSC Ensembl
chr14:25904409..25931895hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3827487
hg1927487
hg1827487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044961, nsv1046399
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)dgv1855n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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