A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3428n100



Internal ID19013796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11802103..11950569hg38UCSC Ensembl
chr19:11912918..12061384hg19UCSC Ensembl
chr19:11773918..11922384hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38148467
hg19148467
hg18148467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057762, nsv1063853
Samples
Known GenesZNF439, ZNF440, ZNF491, ZNF69, ZNF700
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3428n100
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