A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620637



Internal ID21568942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:365640..365640hg38UCSC Ensembl
chrY:276375..276375hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170144
SamplesNA12878
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620637
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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