A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533576



Internal ID21857932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154713958..154714277hg38UCSC Ensembl
chr1:154686434..154686753hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981390
Supporting Variants
Samples
Known GenesKCNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533576
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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