A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv418n209



Internal ID22826493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62106226..62109848hg38UCSC Ensembl
chr12:62500007..62503629hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg383623
hg193623
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5862825, nsv5859085
Samples
Known GenesFAM19A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv418n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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