A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857066



Internal ID22040709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169667698..169667698hg38UCSC Ensembl
chr4:170588849..170588849hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255696
Supporting Variants
Samples
Known GenesCLCN3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857066
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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