A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629813



Internal ID21821860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46506125..46506125hg38UCSC Ensembl
chr19:47009382..47009382hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106799
Supporting Variants
Samples
Known GenesPPP5D1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629813
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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