A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557237



Internal ID21881592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169667680..169667680hg38UCSC Ensembl
chr4:170588831..170588831hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073551
Supporting Variants
Samples
Known GenesCLCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557237
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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