A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415283



Internal ID194543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52082784..52082835hg38UCSC Ensembl
chr16:52116696..52116747hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415283
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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