A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372356



Internal ID22598025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60155942..60196210hg38UCSC Ensembl
chr14:60622660..60662928hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3840269
hg1940269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969495
Supporting Variants
Samples
Known GenesDHRS7
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372356
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