A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4330n100



Internal ID20155946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54034615..54046023hg38UCSC Ensembl
chr20:52651154..52662562hg19UCSC Ensembl
chr20:52084561..52095969hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3811409
hg1911409
hg1811409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060202, nsv1066172, nsv1063512, nsv1065957, nsv1061631, nsv1062635
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)dgv4330n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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