A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742964



Internal ID166630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:22207834..22323613hg38UCSC Ensembl
chrY:24353981..24469760hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38115780
hg19115780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423792
Supporting Variants
Samples
Known GenesLOC100652931, RBMY1F, RBMY2FP, TTTY5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742964
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00251731


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