A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933336



Internal ID22955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49368985..49369309hg38UCSC Ensembl
chr3:49406418..49406742hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447503
Supporting Variants
Samples
Known GenesRHOA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933336
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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