A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552691



Internal ID20925817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43333865..43334893hg38UCSC Ensembl
chr3:43375357..43376385hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260694
Samples
Known GenesSNRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552691
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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