A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929406



Internal ID20329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9926173..9926230hg38UCSC Ensembl
chr3:9967857..9967914hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446315
Supporting Variants
Samples
Known GenesIL17RC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929406
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002342


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