A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886093



Internal ID22661079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69122846..69127767hg38UCSC Ensembl
chr16:69156749..69161670hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg384922
hg194922
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472671
Samples
Known GenesCHTF8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886093
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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