A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6427n54



Internal ID20139851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36353429..36354506hg38UCSC Ensembl
chr19:36844331..36845408hg19UCSC Ensembl
chr19:41536171..41537248hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381078
hg191078
hg181078
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579436, nsv579437
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6427n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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