A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3765n54



Internal ID20137189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73532494..73540730hg38UCSC Ensembl
chr14:73999198..74007434hg19UCSC Ensembl
chr14:73068951..73077187hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg388237
hg198237
hg188237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565137, nsv565122, nsv565120, nsv565121, nsv565130, nsv565123
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3765n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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