A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566383



Internal ID20939454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89255766..89255962hg38UCSC Ensembl
chr9:91870681..91870877hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281367
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566383
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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