A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3778n54



Internal ID22771673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75053172..75058746hg38UCSC Ensembl
chr14:75519875..75525449hg19UCSC Ensembl
chr14:74589628..74595202hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg385575
hg195575
hg185575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565198, nsv565189, nsv565187
Samples
Known GenesACYP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3778n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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