A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1866n100



Internal ID22787953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34638874..34691654hg38UCSC Ensembl
chr14:35108080..35160860hg19UCSC Ensembl
chr14:34177831..34230611hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3852781
hg1952781
hg1852781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038792, nsv1049026
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1866n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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