A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565428



Internal ID20938499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97589104..97589331hg38UCSC Ensembl
chr9:100351386..100351613hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7888n223
Supporting Variantsnssv18281582
Samples
Known GenesTMOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565428
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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