A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942601



Internal ID29069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186309194..186309280hg38UCSC Ensembl
chr3:186026983..186027069hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448053
Supporting Variants
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942601
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00843


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