A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968006



Internal ID22742941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9766605..9801132hg38UCSC Ensembl
chr19:9877281..9911808hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3834528
hg1934528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398325
Samples
Known GenesZNF846
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968006
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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