A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3600n54



Internal ID22771495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28087101..28144861hg38UCSC Ensembl
chr14:28556307..28614067hg19UCSC Ensembl
chr14:27626058..27683818hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3857761
hg1957761
hg1857761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564151, nsv564149
SamplesNINDS_173
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3600n54
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