A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565660



Internal ID20938731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98115591..98116118hg38UCSC Ensembl
chr9:100877873..100878400hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281604
Samples
Known GenesTRIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565660
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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