A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv372n209



Internal ID22826447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:35285313..37010787hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381725475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5907968, nsv5910473, nsv5919866, nsv5922960, nsv5909900, nsv5908875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv372n209
Frequency
Sample Size914
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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