A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417766



Internal ID196955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:5107963..5108727hg38UCSC Ensembl
chrY:4976004..4976768hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738288
Samples
Known GenesPCDH11Y
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417766
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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