A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885158



Internal ID22660142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38n/a
hg19n/a
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variants
Samples
Known GenesDDX19A, DDX19B, LOC100506083
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885158
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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