A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240879



Internal ID20807919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85012372..85013716hg38UCSC Ensembl
chr16:85045978..85047322hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381345
hg191345
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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