A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3519n100



Internal ID19013887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35358159..35370934hg38UCSC Ensembl
chr19:35849061..35861836hg19UCSC Ensembl
chr19:40540901..40553676hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812776
hg1912776
hg1812776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063118, nsv1064016, nsv1065016, nsv1056060, nsv1059785, nsv1065890, nsv1057640, nsv1060131, nsv1056634, nsv1058174
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)dgv3519n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss61
Observed Complex0
Frequencyn/a


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