A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238549



Internal ID20805589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18904876..18905590hg38UCSC Ensembl
chr16:18916198..18916912hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594244
Supporting Variants
Samples
Known GenesSMG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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