A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852601



Internal ID22036244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159705928..159705928hg38UCSC Ensembl
chr2:160562439..160562439hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243332
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852601
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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