A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262836



Internal ID20829876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49837790..49838668hg38UCSC Ensembl
chr3:49875223..49876101hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540576
Supporting Variants
Samples
Known GenesTRAIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262836
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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