A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169273



Internal ID21512731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:16264214..16321104hg38UCSC Ensembl
chrY:18376094..18432984hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3856891
hg1956891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671299
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169273
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