A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710129



Internal ID133795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65229928..65235049hg38UCSC Ensembl
chr16:65263831..65268952hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385122
hg195122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710129
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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