A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262056



Internal ID20829096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33554128..33556566hg38UCSC Ensembl
chr3:33595620..33598058hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg382439
hg192439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552689
Supporting Variants
Samples
Known GenesCLASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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