A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261381



Internal ID20828421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32338128..32339959hg38UCSC Ensembl
chr3:32379620..32381451hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381832
hg191832
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555118
Supporting Variants
Samples
Known GenesCMTM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261381
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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