A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281070



Internal ID20848110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77409630..77482981hg38UCSC Ensembl
chr9:80024546..80097897hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3873352
hg1973352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561296
Supporting Variants
Samples
Known GenesGNA14, VPS13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281070
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00538


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