A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17847633



Internal ID22031276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21726744..21726744hg38UCSC Ensembl
chr16:21738065..21738065hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250161
Supporting Variants
Samples
Known GenesOTOA
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17847633
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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