A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850998



Internal ID22034641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167296465..167296465hg38UCSC Ensembl
chr2:168152975..168152975hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850998
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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