A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742823



Internal ID166489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17451387..18881388hg38UCSC Ensembl
chrY:19563267..21043274hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg381430002
hg191480008
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432002
Supporting Variants
Samples
Known GenesCDY2A, CDY2B, FAM224A, FAM224B, FAM41AY1, FAM41AY2, HSFY1, HSFY2, NCRNA00185, TTTY9A, TTTY9B, XKRY, XKRY2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742823
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00251889


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