A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261386



Internal ID20828426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32519766..32520255hg38UCSC Ensembl
chr3:32561258..32561747hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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