A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265568



Internal ID20474786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48110529..48110529hg38UCSC Ensembl
chr19:48613786..48613786hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765532
Supporting Variants
Samples
Known GenesPLA2G4C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265568
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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