A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706628



Internal ID130294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25619922..25620160hg38UCSC Ensembl
chr16:25631243..25631481hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706628
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.005464


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