A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293869



Internal ID20503087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29990298..29990298hg38UCSC Ensembl
chr3:30031789..30031789hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765589
Supporting Variants
Samples
Known GenesRBMS3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293869
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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