A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5418991



Internal ID198141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15468976..15472351hg38UCSC Ensembl
chrY:17580856..17584231hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg383376
hg193376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5418991
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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