A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560216



Internal ID20933287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91412636..91413368hg38UCSC Ensembl
chr9:94174918..94175650hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281403
Samples
Known GenesNFIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560216
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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