A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852764



Internal ID22036407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142622870..142622870hg38UCSC Ensembl
chr3:142341712..142341712hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254767
Supporting Variants
Samples
Known GenesPLS1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852764
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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