A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937884



Internal ID25971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107224038..107224089hg38UCSC Ensembl
chr3:106942885..106942936hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5407402
Supporting Variants
Samples
Known GenesLINC00882
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937884
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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