A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111334



Internal ID22020567
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 StatusM
Merged Variants
Supporting Variantsnssv17548309
Samples
Known GenesRPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111334
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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