A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv527n209



Internal ID22826602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49646009..49658561hg38UCSC Ensembl
chr13:50220145..50232697hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3812553
hg1912553
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5854112, nsv5854023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv527n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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