A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244420



Internal ID20811460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32217508..32218026hg38UCSC Ensembl
chr17:30544527..30545045hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579460
Supporting Variants
Samples
Known GenesRHOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244420
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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