A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1721n209



Internal ID22827796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161712819..161715772hg38UCSC Ensembl
chr5:161139825..161142778hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382954
hg192954
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5841542, nsv5841522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1721n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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