A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245145



Internal ID20812185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49648828..49649519hg38UCSC Ensembl
chr17:47726190..47726881hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575667
Supporting Variants
Samples
Known GenesSPOP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245145
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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