A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542598



Internal ID317000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49251989..49251989hg38UCSC Ensembl
chr16:49285900..49285900hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707850
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542598
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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