A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279709



Internal ID20846749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117948868..118042557hg38UCSC Ensembl
chr9:120711146..120804835hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3893690
hg1993690
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279709
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00049


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