A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280521



Internal ID20847561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33831512..33831974hg38UCSC Ensembl
chr9:33831510..33831972hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570078
Supporting Variants
Samples
Known GenesUBE2R2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280521
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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