A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419788



Internal ID198911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14048123..14078123hg38UCSC Ensembl
chrY:16160003..16190003hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3830001
hg1930001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738435
Samples
Known GenesVCY, VCY1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419788
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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