A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110465



Internal ID22019698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21574056..23425178hg38UCSC Ensembl
chr19:21756858..23607980hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381851123
hg191851123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634132
Samples
Known GenesLOC100132815, LOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF43, ZNF492, ZNF676, ZNF724P, ZNF728, ZNF729, ZNF730, ZNF91, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110465
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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