A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665177



Internal ID21613482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21539859..21553153hg38UCSC Ensembl
chrY:23701745..23715039hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3813295
hg1913295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170413
SamplesHG00096
Known GenesRBMY1A1, RBMY1B, RBMY1D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665177
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