A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292802



Internal ID20502020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29473228..29473228hg38UCSC Ensembl
chr3:29514719..29514719hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763012
Supporting Variants
Samples
Known GenesRBMS3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292802
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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