A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566024



Internal ID20939095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36238303..37822343hg38UCSC Ensembl
chr9:36238300..37822340hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381584041
hg191584041
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280616
Samples
Known GenesDCAF10, EXOSC3, FBXO10, FRMPD1, GNE, GRHPR, LOC100506710, MELK, MIR4475, MIR4476, MIR4540, PAX5, POLR1E, RNF38, TOMM5, TRMT10B, ZBTB5, ZCCHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566024
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer