A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560543



Internal ID333549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69727903..69728992hg38UCSC Ensembl
chr16:69761806..69762895hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381090
hg191090
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560543
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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