A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845879



Internal ID22029522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50956754..50956754hg38UCSC Ensembl
chr14:51423472..51423472hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258855
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845879
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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