A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669449



Internal ID21617755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:628387..629016hg38UCSC Ensembl
chrY:539122..539751hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170795
SamplesHG03065
Known GenesSHOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669449
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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