A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709163



Internal ID132829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:76007466..76039482hg38UCSC Ensembl
chr16:76041364..76073380hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3832017
hg1932017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709163
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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