A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1244n209



Internal ID22827319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168634546..168636245hg38UCSC Ensembl
chr2:169491056..169492755hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5832005, nsv5831932
Samples
Known GenesCERS6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1244n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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