A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578197



Internal ID20951268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69386211..69387196hg38UCSC Ensembl
chr16:69420114..69421099hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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