A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3520n100



Internal ID19013888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35358159..35387466hg38UCSC Ensembl
chr19:35849061..35878368hg19UCSC Ensembl
chr19:40540901..40570208hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3829308
hg1929308
hg1829308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055725, nsv1064784, nsv1058164
Samples
Known GenesFFAR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3520n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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