A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562081



Internal ID20935152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170268437..170269132hg38UCSC Ensembl
chr3:169986225..169986920hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260505
Samples
Known GenesPRKCI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562081
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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