A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104002



Internal ID22013235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34537754..34750577hg38UCSC Ensembl
chr19:35028659..35241482hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38212824
hg19212824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637085
Samples
Known GenesSCGB1B2P, SCGB2B2, SCGB2B3P, ZNF181, ZNF302
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104002
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