A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707965



Internal ID131631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13859679..13859855hg38UCSC Ensembl
chr16:13953536..13953712hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525858
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707965
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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