A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1854n100



Internal ID20153470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24438841..24524460hg38UCSC Ensembl
chr14:24908047..24993666hg19UCSC Ensembl
chr14:23977887..24063506hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3885620
hg1985620
hg1885620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053330, nsv1039955, nsv1043355
Samples
Known GenesCMA1, KHNYN, SDR39U1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1854n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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