A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv333n209



Internal ID22826408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8804299..8807853hg38UCSC Ensembl
chr12:8956895..8960449hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg383555
hg193555
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5855643, nsv5853228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv333n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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