A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3622n100



Internal ID20155238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50023786..50090736hg38UCSC Ensembl
chr19:50527043..50593993hg19UCSC Ensembl
chr19:55218855..55285805hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3866951
hg1966951
hg1866951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066796, nsv1062689
Samples
Known GenesFLJ26850, VRK3, ZNF473
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3622n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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