A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848801



Internal ID22032444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29249460..29249460hg38UCSC Ensembl
chr16:29260781..29260781hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848801
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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