A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281067



Internal ID20848107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77357323..77358240hg38UCSC Ensembl
chr9:79972239..79973156hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574446
Supporting Variants
Samples
Known GenesVPS13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281067
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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