A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8879n54



Internal ID22776774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:818810..870129hg38UCSC Ensembl
chr4:812598..863917hg19UCSC Ensembl
chr4:802598..853917hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3851320
hg1951320
hg1851320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593224, nsv593225
SamplesHGDP00684
Known GenesCPLX1, GAK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8879n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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