A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419742



Internal ID198867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12613900..12614340hg38UCSC Ensembl
chrY:14725832..14726272hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419742
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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