A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414078



Internal ID193363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9266638..9269135hg38UCSC Ensembl
chrY:9104247..9106744hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg382498
hg192498
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414078
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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