A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742999



Internal ID166665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26625388..26631388hg38UCSC Ensembl
chrY:28771535..28777535hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425602
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742999
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00380469


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