A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622516



Internal ID21814563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15646819..15666334hg38UCSC Ensembl
chr19:15757629..15777144hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3819516
hg1919516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055513
Supporting Variants
Samples
Known GenesCYP4F3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622516
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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