A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707137



Internal ID130803
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 StatusS
Merged Variantsnsv5560543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707137
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.408679


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