A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519679



Internal ID21844038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210106146..210106477hg38UCSC Ensembl
chr2:210970870..210971201hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987434
Supporting Variants
Samples
Known GenesKANSL1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519679
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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