A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4331n100



Internal ID20155947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54034615..54050346hg38UCSC Ensembl
chr20:52651154..52666885hg19UCSC Ensembl
chr20:52084561..52100292hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3815732
hg1915732
hg1815732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067083, nsv1055306
Samples
Known GenesBCAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4331n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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