A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846942



Internal ID22030585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14222901..14222901hg38UCSC Ensembl
chr16:14316758..14316758hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250102
Supporting Variants
Samples
Known GenesMKL2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846942
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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