A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4326n100



Internal ID20155942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54026616..54042100hg38UCSC Ensembl
chr20:52643155..52658639hg19UCSC Ensembl
chr20:52076562..52092046hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3815485
hg1915485
hg1815485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058315, nsv1059551, nsv1067222, nsv1064465, nsv1055799, nsv1060500, nsv1064456
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)dgv4326n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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