A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281476



Internal ID20848516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93448288..93448745hg38UCSC Ensembl
chr9:96210570..96211027hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556315
Supporting Variants
Samples
Known GenesFAM120AOS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281476
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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