A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618976



Internal ID21567281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:526115..526115hg38UCSC Ensembl
chrY:436850..436850hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170833
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618976
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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