A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692648



Internal ID116314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100479861..100480108hg38UCSC Ensembl
chr13:101132115..101132362hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510791
Supporting Variants
Samples
Known GenesPCCA, PCCA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692648
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.115204


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