A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707450



Internal ID131116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52653937..52676665hg38UCSC Ensembl
chr16:52687849..52710577hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3822729
hg1922729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517123
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707450
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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