A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854788



Internal ID22038431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16735824..16735824hg38UCSC Ensembl
chr3:16777331..16777331hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253741
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854788
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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