A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887292



Internal ID22662284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88684919..88686817hg38UCSC Ensembl
chr16:88751327..88753225hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474182
Samples
Known GenesSNAI3, SNAI3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887292
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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