A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3528n54



Internal ID22771423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19821078..19932841hg38UCSC Ensembl
chr14:20289237..20401000hg19UCSC Ensembl
chr14:19359077..19470840hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38111764
hg19111764
hg18111764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563799, nsv563805, nsv563804, nsv563802, nsv563800
Samples
Known GenesOR4K2, OR4K5, OR4N2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3528n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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