A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3441n100



Internal ID20155057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15171818..15199422hg38UCSC Ensembl
chr19:15282629..15310233hg19UCSC Ensembl
chr19:15143629..15171233hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3827605
hg1927605
hg1827605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066831, nsv1056885
Samples
Known GenesMIR6795, NOTCH3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3441n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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