A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672457



Internal ID21620762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:365970..366629hg38UCSC Ensembl
chrY:276705..277364hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170146
SamplesHG00512
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672457
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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