A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239368



Internal ID20806408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59862169..59862467hg38UCSC Ensembl
chr16:59896073..59896371hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239368
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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