A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855848



Internal ID22039491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150207814..150207814hg38UCSC Ensembl
chr3:149925601..149925601hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259796
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855848
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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