A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848633



Internal ID22032276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10960268..10960268hg38UCSC Ensembl
chr2:11100394..11100394hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848633
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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