A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602651



Internal ID21794698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99708212..99708320hg38UCSC Ensembl
chr14:100174549..100174657hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034834
Supporting Variants
Samples
Known GenesCYP46A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602651
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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