A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397333



Internal ID22455203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15694751..15698483hg38UCSC Ensembl
chr19:15805561..15809293hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383733
hg193733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928676
Supporting Variants
Samples
Known GenesCYP4F12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397333
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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