A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244314



Internal ID20811354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69169654..69176437hg38UCSC Ensembl
chr16:69203557..69210340hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg386784
hg196784
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583729
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244314
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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