A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239206



Internal ID20806246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20333884..20334836hg38UCSC Ensembl
chr16:20345206..20346158hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592616
Supporting Variants
Samples
Known GenesUMOD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239206
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer