A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261395



Internal ID20828435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32611483..32612141hg38UCSC Ensembl
chr3:32652975..32653633hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548376
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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