A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929074



Internal ID20094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8569940..8579625hg38UCSC Ensembl
chr3:8611626..8621311hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg389686
hg199686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453284
Supporting Variants
Samples
Known GenesLINC00312
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929074
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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