A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8559n54



Internal ID20141983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126884936..127052770hg38UCSC Ensembl
chr3:126603779..126771613hg19UCSC Ensembl
chr3:128086469..128254303hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38167835
hg19167835
hg18167835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591559, nsv591560, nsv591561, nsv591562
Samples
Known GenesCHCHD6, PLXNA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8559n54
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