A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848780



Internal ID22032423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25497618..25497618hg38UCSC Ensembl
chr16:25508939..25508939hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250194
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848780
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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