A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239888



Internal ID20806928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12820390..12820901hg38UCSC Ensembl
chr16:12914247..12914758hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239888
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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