A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934724



Internal ID23883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62261269..62261320hg38UCSC Ensembl
chr3:62246944..62246995hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5408178
Supporting Variants
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934724
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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