A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244421



Internal ID20811461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32221089..32223709hg38UCSC Ensembl
chr17:30548108..30550728hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382621
hg192621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589843
Supporting Variants
Samples
Known GenesRHOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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