A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542504



Internal ID21866859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22473882..22473882hg38UCSC Ensembl
chr3:22515373..22515373hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542504
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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