A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620190



Internal ID21812237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45400760..45401082hg38UCSC Ensembl
chr19:45904018..45904340hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047239
Supporting Variants
Samples
Known GenesPPP1R13L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620190
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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