A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426994



Internal ID205908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:5105122..5108645hg38UCSC Ensembl
chrY:4973163..4976686hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg383524
hg193524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738287
Samples
Known GenesPCDH11Y
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426994
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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