A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852093



Internal ID22035736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13911882..13911882hg38UCSC Ensembl
chr3:13953379..13953379hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852093
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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