A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260680



Internal ID20827720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42584456..42584854hg38UCSC Ensembl
chr3:42625948..42626346hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539116
Supporting Variants
Samples
Known GenesSEC22C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260680
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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