A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852818



Internal ID22036461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180231349..180231349hg38UCSC Ensembl
chr3:179949137..179949137hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852818
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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