A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620424



Internal ID21568729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9259272..9259272hg38UCSC Ensembl
chrY:9096881..9096881hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg382435
hg192435
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170939
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620424
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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