A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880453



Internal ID22655423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86720556..86725685hg38UCSC Ensembl
chr16:86754162..86759291hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385130
hg195130
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880453
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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