A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853609



Internal ID22037252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190965986..190965986hg38UCSC Ensembl
chr3:190683775..190683775hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853609
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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