A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937792



Internal ID25906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133971099..133971099hg38UCSC Ensembl
chr3:133689943..133689943hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535509
Supporting Variants
Samples
Known GenesSLCO2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937792
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000473


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