A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937785



Internal ID25899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133784938..133786238hg38UCSC Ensembl
chr3:133503782..133505082hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447790
Supporting Variants
Samples
Known GenesSRPRB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937785
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.325367


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