A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742972



Internal ID166638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:22693588..22895281hg38UCSC Ensembl
chrY:24839735..25041428hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38201694
hg19201694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433252
Supporting Variants
Samples
Known GenesTTTY17A, TTTY17B, TTTY17C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742972
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00068918


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