A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1922n100



Internal ID22788009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55941026..55968359hg38UCSC Ensembl
chr14:56407744..56435077hg19UCSC Ensembl
chr14:55477497..55504830hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3827334
hg1927334
hg1827334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042669, nsv1036163
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)dgv1922n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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