A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3494n54



Internal ID22771389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:18504256..19849588hg38UCSC Ensembl
chr14:19280733..20317747hg19UCSC Ensembl
chr14:18350733..19387587hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381345333
hg191037015
hg181036855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563597, nsv563615
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, OR11H2, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3494n54
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