A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3614n100



Internal ID19013982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48224334..48283199hg38UCSC Ensembl
chr19:48727591..48786456hg19UCSC Ensembl
chr19:53419403..53478268hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3858866
hg1958866
hg1858866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061139, nsv1061986, nsv1063977, nsv1061379, nsv1059268
Samples
Known GenesCARD8, LOC100505812, ZNF114
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3614n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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