A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559632



Internal ID20932703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111652251..111652736hg38UCSC Ensembl
chr9:114414531..114415016hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279554
Samples
Known GenesDNAJC25, DNAJC25-GNG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559632
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