A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578860



Internal ID20951931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56467692..56468590hg38UCSC Ensembl
chr16:56501604..56502502hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38899
hg19899
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239300
Samples
Known GenesOGFOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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