A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931909



Internal ID22001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42518750..42518801hg38UCSC Ensembl
chr3:42560242..42560293hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412830
Supporting Variants
Samples
Known GenesVIPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931909
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.235092


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