A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738287



Internal ID161953
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 StatusS
Merged Variantsnsv5426994
Supporting Variants
Samples
Known GenesPCDH11Y
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738287
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000363


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