A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923948



Internal ID16726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222667000..222675628hg38UCSC Ensembl
chr2:223531719..223540347hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg388629
hg198629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440149
Supporting Variants
Samples
Known GenesMOGAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923948
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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