A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5550409



Internal ID323964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24733063..24733105hg38UCSC Ensembl
chr16:24744384..24744426hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706580
Samples
Known GenesTNRC6A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5550409
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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