A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281407



Internal ID20848447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91528347..91529748hg38UCSC Ensembl
chr9:94290629..94292030hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281407
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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