A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv285n97



Internal ID22815682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39368830..39546375hg38UCSC Ensembl
chr8:39226349..39403894hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38177546
hg19177546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154341, nsv1154342, nsv1154338, nsv1154343
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv285n97
Frequency
Sample Size131
Observed Gain0
Observed Loss53
Observed Complex0
Frequencyn/a


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