A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3489n100



Internal ID22789576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:24245189..24413936hg38UCSC Ensembl
chr19:24427991..24596738hg19UCSC Ensembl
chr19:24219831..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38168748
hg19168748
hg18168748
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062684, nsv1062188, nsv1061462, nsv1059986, nsv1065604
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)dgv3489n100
Frequency
Sample Size11257
Observed Gain18
Observed Loss6
Observed Complex0
Frequencyn/a


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