A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567363



Internal ID20940434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111560525..111561391hg38UCSC Ensembl
chr9:114322805..114323671hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279552
Samples
Known GenesPTGR1, ZNF483
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567363
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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