A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706222



Internal ID129888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26542463..26542531hg38UCSC Ensembl
chr16:26553784..26553852hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528158
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706222
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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