A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262063



Internal ID20829103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33651166..33651712hg38UCSC Ensembl
chr3:33692658..33693204hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550885
Supporting Variants
Samples
Known GenesCLASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262063
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00044


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