A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937791



Internal ID25905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133969427..133971110hg38UCSC Ensembl
chr3:133688271..133689954hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563683
Supporting Variants
Samples
Known GenesSLCO2A1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937791
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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