A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1926n100



Internal ID22788013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65789063..65863201hg38UCSC Ensembl
chr14:66255781..66329919hg19UCSC Ensembl
chr14:65325534..65399672hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3874139
hg1974139
hg1874139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038849, nsv1052389
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)dgv1926n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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