A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670157



Internal ID21618464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:365337..365501hg38UCSC Ensembl
chrY:276072..276236hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170143
SamplesHG00513
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670157
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