A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542153



Internal ID21866508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39031609..39031609hg38UCSC Ensembl
chr3:39073100..39073100hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074194
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542153
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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