A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3456n100



Internal ID19013824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19862680..20415952hg38UCSC Ensembl
chr19:19973489..20598758hg19UCSC Ensembl
chr19:19834489..20390598hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38553273
hg19625270
hg18556110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057309, nsv1066446, nsv1066564, nsv1059158
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF253, ZNF486, ZNF682, ZNF826P, ZNF90, ZNF93
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3456n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer