A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259768



Internal ID22064378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:146207782..146207782hg38UCSC Ensembl
chr2:146965350..146965350hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17853829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259768
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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