A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566822



Internal ID20939893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75204344..76674377hg38UCSC Ensembl
chr9:77819260..79289293hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381470034
hg191470034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280993
Samples
Known GenesGCNT1, MIR548H3, PCSK5, PRUNE2, RFK, RPSAP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566822
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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