A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667792



Internal ID21616097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:342498..343578hg38UCSC Ensembl
chrY:253233..254313hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170544
SamplesHG00513
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667792
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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