A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924676



Internal ID17195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203738242..203738293hg38UCSC Ensembl
chr2:204602965..204603016hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398223
Supporting Variants
Samples
Known GenesCD28
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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