A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17847334



Internal ID22030977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81649709..81649709hg38UCSC Ensembl
chr16:81683314..81683314hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250487
Supporting Variants
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17847334
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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