A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv504n209



Internal ID22826579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18196939..18200965hg38UCSC Ensembl
chrUn_gl000212:25691..29717hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384027
hg194027
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5856243, nsv5861984, nsv5859427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv504n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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