A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241388



Internal ID20808428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15379561..15380248hg38UCSC Ensembl
chr17:15282878..15283565hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591902
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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