A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548309



Internal ID21872664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128627052..128657342hg38UCSC Ensembl
chr3:128345895..128376185hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3830291
hg1930291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111334
Supporting Variants
Samples
Known GenesRPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548309
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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