A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280516



Internal ID20489734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29578789..29579111hg38UCSC Ensembl
chr3:29620280..29620602hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750184
Supporting Variants
Samples
Known GenesRBMS3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280516
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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