A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707115



Internal ID130781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69292021..69292670hg38UCSC Ensembl
chr16:69325924..69326573hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515859
Supporting Variants
Samples
Known GenesSNTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707115
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003442


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