A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6425n54



Internal ID20139849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36352224..36353801hg38UCSC Ensembl
chr19:36843126..36844703hg19UCSC Ensembl
chr19:41534966..41536543hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381578
hg191578
hg181578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579430, nsv579429
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6425n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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