A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262852



Internal ID20829892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69159350..69160020hg38UCSC Ensembl
chr3:69208501..69209171hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540006
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262852
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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