A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855919



Internal ID22039562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101048557..101048557hg38UCSC Ensembl
chr4:101969714..101969714hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255058
Supporting Variants
Samples
Known GenesPPP3CA
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855919
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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