A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280182



Internal ID20847222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14329521..14330188hg38UCSC Ensembl
chr9:14329520..14330187hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560717
Supporting Variants
Samples
Known GenesNFIB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280182
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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