A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664725



Internal ID21613031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:26935982..26969365hg38UCSC Ensembl
chr17:25263008..25296391hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3833384
hg1933384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085208
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664725
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