A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11n212



Internal ID22815359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108436096..108437431hg38UCSC Ensembl
chr12:108829873..108831208hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381336
hg191336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6020694, nsv6027700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)dgv11n212
Frequency
Sample Size405
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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