A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16893541



Internal ID169854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198652884..198662554hg38UCSC Ensembl
chr1:198622013..198631683hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg389671
hg199671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439357
Supporting Variants
Samples
Known GenesPTPRC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16893541
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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