A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937631



Internal ID25802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126515388..126515520hg38UCSC Ensembl
chr3:126234231..126234363hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448008
Supporting Variants
Samples
Known GenesUROC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937631
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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