A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854969



Internal ID22038612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62120361..62120361hg38UCSC Ensembl
chr3:62106035..62106035hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254104
Supporting Variants
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854969
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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