A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669083



Internal ID21617388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26652925..26653135hg38UCSC Ensembl
chrY:28799072..28799282hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170515
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669083
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