A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239335



Internal ID20806375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58178604..58179163hg38UCSC Ensembl
chr16:58212508..58213067hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582467
Supporting Variants
Samples
Known GenesCSNK2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239335
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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