A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280079



Internal ID20847119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131365326..131500133hg38UCSC Ensembl
chr9:134240713..134375520hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38134808
hg19134808
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574375
Supporting Variants
Samples
Known GenesPRRC2B, SNORD62A, SNORD62B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280079
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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