A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706251



Internal ID129917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27065688..27087463hg38UCSC Ensembl
chr16:27077009..27098784hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3821776
hg1921776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515970
Supporting Variants
Samples
Known GenesC16orf82
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706251
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000157


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