A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609296



Internal ID21801343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53181757..53181866hg38UCSC Ensembl
chr14:53648475..53648584hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609296
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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