A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708468



Internal ID132134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87400284..87401849hg38UCSC Ensembl
chr16:87433890..87435455hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522094
Supporting Variants
Samples
Known GenesMAP1LC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708468
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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