A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994117



Internal ID21903460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49368985..49369285hg38UCSC Ensembl
chr3:49406418..49406718hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554522
Samples
Known GenesRHOA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994117
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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