A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667953



Internal ID21616260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:368549..368622hg38UCSC Ensembl
chrY:279284..279357hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170150
SamplesHG00731
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667953
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