A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665625



Internal ID21613930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60604527..60613246hg38UCSC Ensembl
chr14:61071245..61079964hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg388720
hg198720
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097900
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665625
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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