A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242998



Internal ID20810038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42330462..42332552hg38UCSC Ensembl
chr17:40482480..40484570hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382091
hg192091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588436
Supporting Variants
Samples
Known GenesSTAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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