A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852284



Internal ID22627219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113719895..113722790hg38UCSC Ensembl
chr8:114732124..114735019hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg382896
hg192896
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852284
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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