A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv416n209



Internal ID22826491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57353109..57355312hg38UCSC Ensembl
chr12:57746892..57749095hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg382204
hg192204
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5855700, nsv5867063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv416n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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