A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv382n209



Internal ID22826457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:37253291..37258231hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5915061, nsv5918304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv382n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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