A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147065



Internal ID346258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77982938..77984141hg38UCSC Ensembl
chr9:80597854..80599057hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381204
hg191204
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026001
Samples
Known GenesGNAQ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147065
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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