A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858833



Internal ID22042476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168030158..168030158hg38UCSC Ensembl
chr5:167457163..167457163hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256433
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858833
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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