A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279552



Internal ID20846592
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 StatusS
Merged Variantsnsv6567363
Supporting Variants
Samples
Known GenesPTGR1, ZNF483
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279552
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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