A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978190



Internal ID22753125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33996548..34013322hg38UCSC Ensembl
chr10:34285476..34302250hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3816775
hg1916775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354700
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978190
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