A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978673



Internal ID22753608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42457884..42511667hg38UCSC Ensembl
chr13:43032020..43085803hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3853784
hg1953784
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371538
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978673
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