A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245284



Internal ID20812324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5398621..5400480hg38UCSC Ensembl
chr17:5301941..5303800hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381860
hg191860
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592150
Supporting Variants
Samples
Known GenesNUP88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245284
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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