A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672202



Internal ID21620507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:368326..368474hg38UCSC Ensembl
chrY:279061..279209hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170149
SamplesHG00731
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672202
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