A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9180n54



Internal ID20142604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101039102..101039683hg38UCSC Ensembl
chr4:101960259..101960840hg19UCSC Ensembl
chr4:102179282..102179863hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38582
hg19582
hg18582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594947, nsv594946, nsv594950, nsv594951, nsv594948, nsv594953
Samples
Known GenesPPP3CA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9180n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss159
Observed Complex0
Frequencyn/a


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