A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625159



Internal ID21817206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46389384..46389384hg38UCSC Ensembl
chr19:46892641..46892641hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112445
Supporting Variants
Samples
Known GenesPPP5C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625159
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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