A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958390



Internal ID39575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169648798..169653064hg38UCSC Ensembl
chr4:170569949..170574215hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg384267
hg194267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469939
Supporting Variants
Samples
Known GenesCLCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958390
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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